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“OPHTHALMOLOGY”
Active Recall Based
Integrated Edition
Published by Delhi Academy of Medical Sciences (P) Ltd.

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ISBN : 978-93-89309-25-6

First Published 1999, Delhi Academy of Medical Sciences

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 Contents
Chapter 1 Anatomy and Embryology 1 – 11
Chapter 2 Lens 12 – 36
Chapter 3 Cornea and Sclera 37 – 63
Chapter 4 Conjunctiva 64 – 82
Chapter 5 Retina 83 – 116
Chapter 6 Neurophthalmology 117 – 140
Chapter 7 Glaucoma 141 – 168
Chapter 8 Orbit 169 – 191
Chapter 9 Eyelids and Lacrimal drainage system 192 – 214
Chapter 10 Uvea 215 – 234
Chapter 11 Squint 235 – 256
Chapter 12 Optics 257 – 284
 1 AnAtomy And Embryology

CONCEPTS
 Concept 1.1 Basic anatomy

 Concept 1.2 Vascular and lymphatic supply

 Concept 1.3 Embryology

2 | Ophthalmology
Concept 1.1: Basic anatomy
Learning objectives
ƒ To know about layers of eye and its components
ƒ To learn about chambers and segments of eye

Time Required
1 reading
st
20 mins
2nd look 5 mins

Basic Anatomy
The eye is placed in a bony socket called the orbit
Three parts – outer fibrous, middle vascular, inner neural

Fig.1.1:

Outer Fibrous:
Anterior 1/6th — transparent cornea, posterior 5/6th opaque sclera. Junction is called
limbus

Middle Vascular (Uveal Tissue):

From anterior to posterior, it consists of iris, ciliary body and choroid
 Anatomy and Embryology | 3
Iris: Controls amount of light entering the eye
Ciliary body: aqueous humour production, accommodation
Choroid: supplies oxygen and nutrition to outer layers of retina

Inner Neural (Retina):

It extends from the optic disc posteriorly to the ora serrata anteriorly

Anterior and Posterior Chambers (Anterior Segment)

There are two fluid filled areas in the eye – known as the anterior and posterior chambers.
The anterior chamber is located between the cornea and the iris, and the posterior
chamber between the iris and ciliary processes.
The vitreous cavity (Posterior segment) lies between the lens and the back of the
eye. A jellylike substance called vitreous humor fills the cavity, nourishing the inside of
the eye and helping the eye hold its shape.
4 | Ophthalmology
Concept 1.2: Vascular and lymphatic supply
Learning Objectives
ƒ To know major vessels supplying eye structures

Time Required
1st reading 20 mins
2 look
nd
10 mins

The eyeball receives arterial blood primarily via the ophthalmic artery. (branch of the
internal carotid artery)
The ophthalmic artery gives rise to many branches, which supply different components
of the eye.
• The central artery of the retina is the most important branch – supplying the internal
surface of the retina.

Fig.1.2:

• The ciliary arteries are divisible into three groups, the long posterior, short posterior,
and the anterior.
A. Short posterior ciliary arteries -
2 trunks from ophthalmic artery
↓
Each trunk divides into 10-20 branches
↓
Pierce sclera around optic nerve
Supplies the choroid
B. Long Posterior ciliary Arteries –
2 in number
Nasal and Temporal
↓
 Anatomy and Embryology | 5
Run in suprachoroidal space to reach the ciliary muscle
↓
Anastamose with each other and anterior ciliary arteries
↓
Major Arterial Circle – [Circulus Arteriosus Major] (At root of iris)
C. Anterior ciliary Arteries – (7)
Derived from muscular branches of ophthalmic artery
↓
Pass anteriorly in episclera
↓
Give branches to sclera – limbus and conjunctiva
↓
Pierce sclera near limbus to enter ciliary muscle
↓
form Major Arterial Circle
↓

Some branches Branches run supply ciliary radially through

iris processes towards pupillary margin to
form ‘Circulus arteriosus minor’.
Venous drainage of the eyeball is carried out by vortex veins, central retinal vein into
the superior and inferior ophthalmic veins. These drain into the cavernous sinus, a dural
venous sinus behind the eye.

LYMPHATIC DRAINAGE

Fig.1.3:

From lateral half – into preauricular nodes

From medial half – submandibular nodes
6 | Ophthalmology
Concept 1.3: Embryology
Learning objectives
ƒ To learn about derivatives of eye and its implications

Time Required
1st reading 30 mins
2nd look 10 mins

Surface Ectoderm Neural Ectoderm Mesoderm Neural Crest

• Conjunctival • Iris and • Extraocular • Corneal stroma keratocytes and endothelium

and corneal ciliary body muscles • Sclera
epithelium epithelium • Temporal Sclera • Iris stroma
• Lacrimal • Retina • Vascular
glands • Ciliary muscles
• Smooth muscle endothelium of
• Eyelid of Iris eye and orbit • Choroidal stroma
skin and • Optic nerve • Part of vitreous • Trabecular meshwork
appendages • Orbital bones
• Part of the
• Lens vitreous • Orbital connective tissue
• Connective tissue sheath and muscular layer of
ocular and orbital blood vessels
• Uveal and conjunctival melanocytes
• Meningeal sheaths of optic nerve
• Schwann cells of ciliary nerves
• Ciliary ganglion

Formation of OPTIC VESICLE and STALK

Neural plate

A
Thickening

Optic sulcus
C

Optic veside
D

Prosencephalon

E F
H
Optic vesicle

Optic stalk

Optic vesicle
G H

Fig.1.4:
 Anatomy and Embryology | 7
During the folding of the neural tube, a ridge of cells comprising the neural crest develops
from the tips of the converging edges and migrates to the dorsolateral aspect of the
tube. Neural crest cells from this region subsequently migrate and give rise to various
structures within the eye and the orbit.

FORMATION OF LENS VESICLE AND CUP

Fig.1.5:

DEVELOPMENT OF LENS FIBRES

Fig.1.6:

Hyaloid vasculature
Hyaloid vessel extends from the optic disc through the vitreous humor to the lens.
It starts regressing at 4 months and disappear by 8th month.
• Persistence after birth is called Persistent Hyperplastic primary vitreous.
• Anterior remnant of hyaloid artery is known as Mittendorf spots and posterior remnant
of hyaloid artery is known as Bergmeister’s papilla.
8 | Ophthalmology

Fig.1.7: Persistent Hyperplastic primary vitreous

Fig.1.8: Mittendorf dot Fig.1.9: Bergmister papilla

 Anatomy and Embryology | 9
Coloboma
Colobomas due to defective closure of the embryonic cleft. Typical coloboma occur in
the lower part of the eye.

Fig.1.10:

Fig.1.11: Iris coloboma Fig.1.12: Eyelid coloboma

Fig.1.13: Lens coloboma Fig.1.14: Choroid coloboma

10 | Ophthalmology
Worksheet
• DO THIS CHAPTER FROM DQB

• EXTRA POINTS FROM DQB


 Anatomy and Embryology | 11
• Name the structures of eye in the pic

e
a
b
c
d

• Name derivatives of Surface ectoderm

• Identify _________________

• Identify _________________
 2 Lens

CONCEPTS
 Concept 2.1 Anatomy, Physiology and
Investigations

 Concept 2.2 Etiology of cataracts

 Concept 2.3 Senile Cataract

 Concept 2.4 Management of Cataract

 Concept 2.5 Complications of Cataract Surgery

 Concept 2.6 Congenital Anomalies and

Ectopia lentis
 n
Concept 2.1: Structure and physiology of lens
Learning objectives
ƒ To know basic lens anatomy and physiology

Time Required
1 reading
st
20 mins
2nd look 10 mins
• 80% glucose is metabolized anaerobically.
• Lens derives its nutrition from aqueous humour.
• Antioxidant system of the lens constitutes: Vitamin C, vitamin E, and glutathione.
• Weigerts Ligament - It is adhesion between lens and anterior vitreous (hyaloid)
• Zonules of lens are suspensory ligaments which support the lens.

Anatomy:
Biconvex.
Diameter: 9-10 mm.
Refractive index: 1.39
Total power : 16-17 D.
Two surfaces:
Anterior and Posterior.
Anterior surface has a radius of curvature of 10 mm while posterior surface has 6mm
(more convex and stepper than anterior surface).
Lens capsule Thickest - pre - equator Thinnest - At
poles- thinnest at posterior pole.
Anterior epithelium Single layer of epithelial cells.
Cuboidal cells at centre.
Anterior capsule
Become columnar at periphery.
ens fibres ucleus old lens fibers Anterior epithelium

mbryonic months of gestation

oetal months of gestation till birth
Cortex
nfantile birth to puberty
dult puberty to rest of life . Adult
Nucleus

ortex youngest lens fibers . Infantile

Foetal
Parts of nucleus: Embryonic
1. Embryonic nucleus
2. Fetal nucleus
3. Infantile nucleus
4. Adult nucleus

Fig.2.1:
 Ophthalmology
Concept 2.2: Etiology of cataracts
Learning objectives
ƒ To know and identify different types of congenital and acquired cataracts
ƒ To learn morphologies of various cataracts

Time Required
1 reading
st
40 mins
2 look
nd
15 mins

Congenital and Developmental Cataract:

Etiology:
Idiopathic Heredity: Maternal Factors: Malnutrition. Foetal or Infantile Factors:
Usually dominant. TORCH infections. Metabolic :
Drugs: Thalidomide, corticosteroids • Galactosemia.
radiation.
Congenital anomaly:
• Lowe’s syndrome.
• Myotonia dystrophica.

Birth Trauma.
Malnutrition.

Types of Congenital and Developmental Cataract: cryg gene

1. Punctate Cataract:
a. Blue dot cataract: Most common

Fig.2.2:
 n
b. Sutural cataract/Anterior axial embryonic cataract: When these blue dots are
crowded in the Y sutures.
c. Cataracta centralis pulverulenta: Central sphenoidal or biconvex opacity consisting
of powdery fine white dots within the embryonic or fetal nucleus.
2. Zonular Cataract (Lamellar Cataract):
Most common type of congenital cataract causing diminution of vision
• In foetal nucleus.
• Small linear opacities towards equator – Rider and spokes

Fig.2.3:

Acquired Cataracts:
Diabetic Cataract
• Snow-flake or snow-storm cataract
• Sorbitol accumulation in lens due to aldose reductase pathway leads to overhydration
of lens

Fig.2.4:
 Ophthalmology
Traumatic Cataract (Blunt Trauma): Rosette shaped cataract

Fig.2.5:

Vossius ring – iris pigments on lens capsule after blunt trauma

Fig.2.6:

Radiational Cataract: Glass Blower’s or Glass- worker’s cataract

Wilson’s disease:
• Hepatolenticular degeneration
• Sunflower cataract

Fig.2.7:
 n
• Kayser – Fleischer Ring: In Descement’s membrane of cornea

Fig.2.8:

Myotonic dystrophy: Christmas tree cataract

Fig.2.9:

Atopic dermatitis: Shield cataract

Fig.2.10:
 Ophthalmology
Galactosaemic cataract:
• Deficiency of GP T Galactose ridyl Transferase : Oil-droplet cataract

Fig.2.11:

• Deficiency of Galactokinase: amellar cataract

Lowe’s syndrome (Oculo- cerebro-renal syndrome):

• Congenital cataract. Glaucoma, Microphakia
• Posterior lenticonus

Complicated Cataract: develops as a result of some other primary ocular

disease like
• veitis

Fig.2.12:

• Degenerative – Myopia, Retinitis pigeentosa

• Tumours
 n
Drugs causing Cataract:

Steroids
Miotics
hlorproma ine henothia ines
Gold
Busulphan
Amiodarone

Morphologies of cataracts

Fig.2.13:

Anterior capsular/polar cataract: due to corneal perforation (penetrating injury)

Posterior polar cataract- due to persistence of posterior part of the vascular sheath
of lens
Anterior subcapsular cataract – Amiodarone, shield, Chlorpromazine
Posterior subcapsular cataract – Steroids, radiation, busalphan
 Ophthalmology
Concept 2.3: Senile Cataract
Learning objectives
ƒ To know and identify different types and stages of senile cataract

Time Required
1 reading
st
20 mins
2nd look 10 mins

Senile Cataract:
Stages of maturation of cortical cataract
NUCLEAR CORTICAL

Increased age related Decreased level of total

nuclear sclerosis proteins, amino acids
and potassium
+
Increased insoluble Increased concentration
proteins of Sodium

Deposition of Melanin Hydration and

and Urochrome conagulation of
Pigments proteins

Cuneiform-
Radial Spokes and
Cupulliform-Posterior
subcapsular

Fig.2.14:

Nuclear sclerosis
• Second sight phenomeon (due to myopic shift)
• Vision improves with pin hole

Nuclear sclerosis Type of Cataract

Brown Cataracta brunescens
Black Cataracta nigra
Red Cataracta – rubra
Nuclear cataract
• Hemeralopia (day blindness)
• Vision does not improve with pin hole
 n

Fig.2.15: Nuclear Sclerosis Fig.2.16: Cuneiform cataract

Fig.2.17: Posterior Subcapsular Cataract

Fig.2.18:

Incipient/Intumuscent stage – frequent change of glasses, coloured haloes

Fincham’s Test differentiates haloes between cataract and angle closure glaucoma
 Ophthalmology
Concept 2.4: Management of Cataract
Learning objectives
ƒ To know about different surgeries to manage cataract
ƒ To learn steps of phacoemulsification
ƒ To know different O s used in cataract surgery

Time Required
1 reading
st
45 mins
2 look
nd
15 mins

There is no role of medical therapy in cataract

Surgeries:
Congenital Acquired
• Mydriatics/ Optical iridectomy for stationary • ntracapsular cataract extraction
central cataracts • xtracapsular cataract extraction
• Lens aspiration with primary posterior • Small incision cataract surgery S S
capsulotomy with anterior vitrectomy • Phacoemulsification.

Anaesthesia In Cataract Surgery:

It can be of following types:
Topical Commonly paracaine eye drops are
used
Peribulbar In peribulbar space around the eyeball
Retrobulbar space behind the equator of the eye Greater risk of retrobulbar haemorrhage,
globe perforation and optic nerve
damage.
The last muscle to be rendered akinetic is superior oblique, as it is supplied by the fourth
nerve which is outside the muscle cone

Steps of Phacoemulsification
1. Preparation
ƒ Retrobulbar, peribulbar or topical anesthesia
2. Clear corneal tunnel/Limbal incisiom
ƒ Stab incision with 2.75-3.2 mm keratome for main wound
3. Fill anterior chamber with viscoelastic
4. Continuous circular capsulorrhexis- trypan blue dye can be used
5. Hydrodissection (cleavage between cortex and capsule) and hydrodelineation
(cleavage between nucleus and epinucleus)
 n

Fig.2.19:

6. Phacoemulsification of nucleus

Fig.2.20:

Fig.2.21:
 Ophthalmology
7. Soft lens aspiration
ƒ Aspirate soft lens with automated infusion- aspiration cannula
. O implantation
ƒ nsert foldable O into capsular bag
9. Wound closure if necessary

FEMTOSECOND LASER ASSISTED CATARACT SURGERY (FLACS)-

The femtosecond laser (1053 nm wavelength) can be used to create cleavage planes via
photodisruption in tissues. sed for craeting
• Wounds
• Anterior capsulotomies
• Nuclear fragmentation
Also used in keratoplasty and arcuate keratotomies

Other cataract surgeries

Fig.2.22: Extracapsular Catract Extraction (ECCE)

Fig.2.23: SICS
 n

Fig.2.24: ICCE

Intra Ocular Lens (IOLs):

deal site of O implantation is Posterior Chamber.
Non-foldable lenses-PMMA.
Foldable lenses are: Hydrogel, Silicon, Acrylic.

Fig.2.25:

PCIOL
AC- O . – examples are elman multiflex., ris-supported-worst’s or Singh’s iris claw
lens
 Ophthalmology

Fig.2.26: ACIOL

Fig.2.27: Scleral fixated IOL (placed behind iris, done when there is no posterior capsule support)

Biometry:
• t is the process of calculating the power of O

SRK Formula:
• P= A-2.5L-0.9 K
A= constant
L=Axial length
K= Curvature of cornea
 n

Fig.2.28: ULTRASOUND A and B scan

Fig.2.29: Keratometry
 Ophthalmology
Concept 2.5: Complications of Cataract Surgery
Learning objectives
ƒ To learn about various complications during and after cataract surgery

Time Required
1st reading 30 mins
2 look
nd
10 mins

Complications of Cataract Surgery:

Operative Early Post- Late Post-Operative IOL-Related
Operative
Irregular incision. Hyphema. After cataract UGH syndrome
Injury to cornea, Iris prolapse. Cystoid macular edema Malpositions of IOL.
Descment detachment.
Iris injury and
iridodialysis.
Accidental rupture of Bullous keratopathy Bullous keratopathy Toxic anterior
lens capsule. Vitreous segment syndrome
loss. SS
Expulsive suprachoroidal Endophthalmitis Retinal detachment
haemorrhage.
Malignant glaucoma Endophthalmitis
Pupil block glaucoma Epithelial in-growth.
Fibrous down growth
• Endophthalmitis. Most common organism is Staphylococcus epidermidis.
• ost common late complication is –After cataract / Posterior capsular opacification/
Elschnig’s Pearls and Soemmerings Ring- treatment by laser capsulotomy (Nd- YAG
laser)

Fig.2.30: Elschnig pearls Fig.2.31: Posterior capsular opacification

 n

Fig.2.32: Pupil block GLAUCOMA

Cornea
Ciliary Body

Aqueous
Lens

Vitreous

Aqueous

Fig.2.33: AQUEOUS MISDIRECTION SYNDROME/ MALIGNANT GLAUCO

 Ophthalmology
Concept 2.6: Congenital Anomalies and Ectopia lentis
Learning objectives
ƒ To know some terms of congenital anamoly of lens
ƒ To learn about causes of subluxation

Time Required
1 reading
st
20 mins
2nd look 10 mins

Congenital Anomalies of Lens:

Coloboma ailure to close embryonic fissure
Lenticonus Anterior - Alports Syndrome.
Posterior - Lowes Syndrome.
Microphakia Lowe’s syndrome - lens small and disc like
Micro spherophakia Small and spherical lens:
Weil Marchesani Syndrome.

Fig.2.34: Lens coloboma

Fig.2.35: Anterior and posterior lenticonus

 n
Ectopia lentis
Subluxation is displacement of the Lens in patellar fossa
Simple Ectopia Lentis Symmetrical and upwards.
Ecoptia lentis et pupillae Pupil displaced in direction opposite to the lens.

Marfans syndrome Upwards and temporal

Homocystinuria Down and nasally

Sulphite oxidase deficiency

Hyperlysinaemia

Aniridia

Well-Marchesani syndrome Inferior subluxation

Microspherophakia. anterior dislocation

Fig.2.36: Subluxation of lens in Marfans

Fig.2.37: Anterior dislocation of lens

 Ophthalmology
Worksheet
• DO TH S CHAPTE F O D B

• E T A PO NTS F O D B


 n
• Oldest lens fibres are
• Antioxidant system of the lens constitutes
• ider and spokes are seen in
• dentify -

Write the name of cataract morphologies in boxesSteps of phacoemulsification

 Ophthalmology

1
2
3
4
5
6
7
8
• SRK Formula
• deal site of O implantation is
• Treatment of this complication of cataract surgery is

• Identify -
 n
• Identify the IOL -

List some causes of subluxation of lens

1

5
Ophthalmology
EXTRA POINTS:
 3 Cornea and SClera

CONCEPTS
 Concept 3.1 Anatomy, Physiology and
Investigations

 Concept 3.2 Infective keratitis

 Concept 3.3 Corneal Degenerations and

depositions

 Concept 3.4 Corneal ectasias

 Concept 3.5 Corneal Dystrophy

 Concept 3.6 Keratoplasty

 Concept 3.7 Sclera

38 | Ophthalmology

Concept 3.1: Anatomy, Physiology and Investigations:

Learning objectives
ƒ To know basic cornea anatomy and physiology
ƒ To know about some special investigations of cornea

Time Required
1 reading
st
30 mins
2 look
nd
10 mins

t is a transparent, avascular structure, forming 1/6th of the outer fibrous coat of eyeball
Horizontal diameters -11.7 mm.
Vertical diameter of anterior surface is 10.6 mm while that of posterior is 11.7 mm.
Refractive power: 43-45D
Refractive index: 1.376.

Structure:
t consists of six distinct layers from anterior to posterior :

Fig.3.1:
 orn a and l ra | 39
• Epithelium.
• Bowman’s membrane, Not a true membrane but a condensed superficial part of
stroma.
• Stroma: 90 % thickness
• Dua’s layer
• Descemet’s membrane: Ends at the anterior limit of trabecular meshwork as
Schwalbe’s ring.
• Endothelium.

Physiology:
Cornea is avascular, dehydrated, transparent structure with aerobic metabolism.
Factors Responsible for Maintaining the Transparency of Cornea:
1. Epithelium :. ade up of stratified squamous non-keratini ed epithelial cells. Have
microvilli.
2. Stroma: regular arrangement of collagen fibrils in a lattice form separated from
each other by less than the wavelength of light 000- 000A . Stroma pressure has
also role in maintain transparency.
3. Endothelium: barrier function and pump function. t has Na / ATPase pump.
ade up of a single layer flat polygonal cells. Cell density in young adults is 000
cells/mm2. The most metabolically active layer of cornea is endothelium.
4. Avascular cornea

Nervous supply

Fig.3.2:
40 | Ophthalmology
Special investigations related to cornea:
Pachymetry Measures cornea thickness
Specular microscopy Evaluates corneal endothelium
Keratometry Measures corneal curvature
Keratoscopy/Placido disc/ Topography Detects abnormalities of corneal shape
Vital stainings Flourescein stain stains corneal defects
Rose-Bengal stain: It stains dead cells and mucous

Placido disc

Normal Aspheric cornea eratoconus

Fig.3.3:

Fig.3.4: SPECULAR MICROSCOPY and normal endothelial cells

Fig.3.5: AESTHESIOMETER
 orn a and l ra | 41
Concept 3.2: Infective keratitis/Corneal ulcer:
Learning objectives
ƒ To know and identify various forms of infective keratitis
ƒ To learn about different corneal opacities

Time Required
1 reading
st
60 mins
2nd look 20 mins

General symptoms
atering, photophobia 1st , redness, pain, mild discharge, diminuition of vision

Fig.3.6: FUNGAL CORNEAL ULCER Fig.3.7: FUNGAL CORNEAL ULCER with hypopyon

Fig.3.8: ACANTHAMOEBA KERATITIS Fig.3.9: BACTERIAL CORNEAL ULCER

Fig.3.10: HERPES SIMPLEX Fig.3.11:

Dendritic ulcer
42 | Ophthalmology

Fungal Acanthamoeba Viral Bacterial

Organism Most common Protozoa Herpes Most common in India is:
in India is: simplex>Herpes Staphylococcus epidermidis
Aspergillus zoster
fumigatus
Pseudomonas (MC cause of
keratitis in contact lens users).
Important Trauma by a Soft contact lens
Pedisposing vegetative matter wearers who use tap
factor water for cleaning
the lenses
Special clinical Signs are more Symptoms are more Decreased corneal Pathogens which can penetrate
features than symptoms than signs sensations intact corneal (epithelium) are:
• Neisseria gonorrheae/
Ulcer – dry and Blurred vision Epithelium meningitis
rough. and pain are involement- • Corynebacterium
Stromal infiltrates characteristically Dendritic ulcer: The diphtheriae.
with feathery severe and bed of ulcer stains • Listeria.
hyphate edges disproportionate with
• Haemophilus
to the extent of uorescein and
Satellite lesions
ocular involvement. virus laden cells at
in periphery.
This occurs due to the margin of ulcer Pneumococcal keratitis is
Associated perineural invasion called ‘Hypopyon Corneal
take up Rose Bengal
hypopyon: Ulcer’and the ulcer is called
stain.
Unsterile. “Ulcus serpens”.
Multifocal patchy
anterior stromal Stromal involement-
infiltrates which Due to direct
gradually enlarge viral invasion and
and coalesce to form destruction. Stroma
are complete, central has cheesy, necrotic
or paracentral non- appearance with
suppurative ring associated uveitis.

Pseudo dendrites. Interstitial keratitis

– hypersensitivity
reaction to virus,
Salmon patch seen

Endothelium
Involvement –
Disciform ulcer,

Trophic ulcer - also

called Metaherpetic
keratitis- due to
denervation and
drug toxicity.
 orn a and l ra | 43

Corneal Smear Smear Examination: PCR Gram stain

scraping sample examination: alco our white, Blood/Choclate agar
KOH wet Acridine orange
preparation. Culture medium:
Gomori’s Non-Nutrient Agar
methamine silver with E coli.
stain.
Culture:
Saboraud’s
glucose agar.
Treatment Topical 5% Combination of Epithelium – topical ortified topical antibiotics
Natamycin propamidine and Acyclovir a. Tobramycin : 13 mg/ml.
polyhexamethylene
b. Cefazoline : 50 mg/ml.
biguanide eye drops.
Others Interstitial and
Other drugs: disciform – topical
a. Topical :
Fluconazole a. chlorhexidine steroids
(0.2%) 0.02%,
b. Oral: b. neomycin 0.175% Trophic – stop
Fluconazole, c. clotrimazole 1% causative drug,
iatraconazole. d. Miconazole 1%. lubricants

Steroids are
contraindicated in
epithelial keratitis
Topical cycloplegics are adjuvant treatment for keratitis

HERPES ZOSTER KERATITIS

Hutchisons rule / sign: hen the tip of the nose is involved then eye will be involved.
This is because the involvement of nasocilliary nerve is generally associated with ocular
complications
Ocular Lesions
External Lesions:
• Conjunctivitis.
• Episcleritis.
• Scleritis – less common.
Corneal Lesions:
• Punctate epithelial keratitis
• ay be associated with filamentary keratitis.
• icro dendritic ulcers Pseudodendrites .
• Nummular eratitis – involves superficial stroma.
• Disciform keratitis. Anterior uveitis.
Neurological Complications:
• Cranial nerve palsies – all 3rd, 4th and 6th can be involved.
• Optic neuritis.
• Encephalitis.
• Contralateral hemiplegia.
44 | Ophthalmology

Fig.3.12:

Interstitial Keratitis:
t is an inflammation of the corneal stroma with no primary involvement of the epithelium
or endothelium.

Fig.3.13:

Salmon patch –Interstitial keratitis

Causes:
1. Congenital syphilis: Deep vessels Ghost vessels – Salmon – patch .
2. Tuberculosis.
. Cogan’s syndrome: nterstitial keratitis associated with deafness.
4. Sarcoidosis.
5. eprosy.
6. Filiariasis

Moorens Ulcer:
t’s a peripheral ulcerative keratitis caused by ischemic necrosis caused by vasculitis of
limbal vessels. asculitis occurs due to the en yme collagenase and proteoglyconase
produced from adjacent conjunctiva. t is of two types:
• imited form: sually unilateral and affects the elderly.
• Progressive form: sually bilateral and affects the young individuals.
 orn a and l ra | 45
Corneal Opacities:
1. Nebula: superficial scars involving bowman’s layer and superficial stroma less than
1/3rd . Treatment is keratectomy by excimer laser or by lamellar keratoplasty.
2. acular opacity: Semi dense opacity resulting from scarring of about 1/ rd to 2/3rd
cornea stroma. Treatment is optical iridectomy or by keratoplasty.
. eucoma: Dense opacity resulting from scarring of more than 2/ rd of stroma.
Treatment is same as acular one.
. Adherent leucoma: Healing occurs after perforation of cornea with incarcination of
iris.

Fig.3.14:

Neurotrophic Keratopathy: oss of neural influence causes edema and exfoliation of

epithelial cell
• HSV.
• HZO.
• DM.
• eprosy.
• Section of Vth nerve.

Photophthalmia:
eratoconjunctivitis due to exposure of rays especially from 11 to 2 0 nm
46 | Ophthalmology
Concept 3.3: Corneal Degenerations and depositions:
Learning objectives
ƒ To know and identify various degenerations of cornea
ƒ To learn the layers in which depositions are seen in various conditions

Time Required
1 reading
st
30 mins
2 look
nd
10 mins

Arcus Senilis:
Bilateral lipid deposition starting in superior and inferior perilimbal cornea and progress
circumferentially to form 1 mm wide band.
Age related or it may be associated with hyper lipoproteinaenmia

Fig.3.15:

Band –Shaped Keratopathy:

t is the deposition of calcium on the cornea in the shape of a band.

Etiology:
1. Pthisis bulbi.
2. Chronic uveitis in children.
. Hypercalcemia.
4. Idiopathic.
Treatment: Chelation which is done with EDTA

Fig.3.16: Band shaped keratopathy

 orn a and l ra | 47
Corneal Pigmentations and depositions:
Iron (Epithelial Deposition):
Fleischer’s ring Keratoconus.
Hudson-Stahli line Idiopathic.
Stocker’s line Pterygium.

Ferry’s line Filtering bleb.

Siderosis Iron foreign body

Silver In Agyrosis in descement’s membrane.

Gold In Chrysiasis in the epithelium and stroma
Copper In Wilson’s disease [Kayser- Fleischers ring] In descement’s membrane.
Melanin In pigment dispersion syndrome [Krukenberg spindle] in the endothelium.
Drugs Vortex keratopathy in the epithelium
(Amiodarone/Chloroquine/NSAIDs)
whorled pattern
Protein Spheroidal degeneration In anterior stroma
Hyaline Salzman nodular generation Superficial stromal opacities

Fig.3.17: KAYSER –FLEISHER RING Fig.3.18: VORTEX KERATOPATHY

Fig.3.19: SPHEROIDAL DEGENERATION Fig.3.20: SALZMAN NODULAR

DEGENERATION
48 | Ophthalmology
Concept 3.4: Corneal ectasias:
Learning objectives
ƒ To know various corneal thinning disorders of cornea
ƒ To learn about signs keratoconus and its management

Time Required
1 reading
st
30 mins
2 look
nd
15 mins

Ectatic Degenerations:
a. eratoconus.
b. eratoglobus.
c. Pellucid marginal degeneration
d. Terriens marginal degeneration

Keratoconus:
Non-inflammatory, usually bilateral ectasia of the cornea giving it a conical shape with
resultant myopia with irregular astigmatism.
Keratoconus – Clinical features
Symptom Impaired vision due to progressing myopia and irregular
astigmatism
Uniocular diplopia
Slit–lamp examination Vogt’s Striae
Prominent corneal nerves
Hurricane keratopathy - Whorl pattern of sub-
epithelialkeratopathy due to effect of contact lens.
Retinoscopy Scissors re ex awning re e
Keratometry Irregular astigmatism
Keratoscopy Irregularity
Munsons Sign V-shaped deformity of lower lid in down gaze
Fleischers ring Iron deposition in epithelium
Acute hydrops Sudden hydration of corneal stroma due to rupture of
Descements membrane.
Investigations: Corneal topographic is diagnostic Pentacam/Orbscan

Treatment:
Astigmatic spectacles igid gas permeable contact lens GPs collagens crosslinking
C Penetrating eratoplasty.
 orn a and l ra | 49

Fig.3.21: Keratoconus Fig.3.22: FLEISHER RING under

Cobalt blue light

Fig.3.23: Fig.3.24: OIL DROPLET REFLEX

Fig.3.25: VOGT’s striae Fig.3.26: PROMINENT CORNEAL NERVES

50 | Ophthalmology
Concept 3.5: Corneal Dystrophy:
Learning objectives
ƒ To know various corneal dystrophies and their salient features

Time Required
1 reading
st
40 mins
2nd look 10 mins

Corneal Dystrophy:
Group of spontaneous appearing, usually inherited, bilateral, stationary or slowly
progressive corneal alterations that develop in absence of inflammation.
Corneal Dystrophies
Layer Dystrophy Causative Inheritance Deposit
gene characteristics

Epithelial - Microcystic (Cogans) TGFb1 Limited familial cases ot like or finger

subepithelial (epithelial basement print
membrane) KRT3 Autosomal dominant
Meesmann’s Tiny epithelial
cysts.
Epithelial - Reis – Buckler’s TGFb1 Autosomal dominant Lack of
stromal Lattice TGFb1 Autosomal dominant hemidesmosomes
Granular TGFb1 Autosomal dominant amyloid
hyaline
Stromal Macular CHST6 Autosomal recessive Mucopoly
saccharodosis
Endothelial Fuch’s endothelial COL8A2 Autosomal dominant corneal guttatae
Posterior COL8A2 Autosomal dominant Vesicular
polymorphous or band-like
opacities
 orn a and l ra | 51

Fig.3.27: Cogan microcystic Fig.3.28: Meesman

Fig.3.29: Reis – Buckler

Fig.3.30: LATTICE TYPE

52 | Ophthalmology

Fig.3.31: GRANULAR TYPE

Fig.3.32: MACULAR TYPE

Fig.3.33: ENDOTHELIAL CORNEAL DYSTROPHY : FUCH’S DYSTROPHY

 orn a and l ra | 53
Concept 3.6: Keratoplasty:
Learning objectives
• To know various types of keratoplasty and their indications

Time Required
1 reading
st
25 mins
2nd look 10 mins

Keratoplasty:
eplacement of diseased cornea by a graft of homologous tissue. t is of two types
i.e. penetrating and lamellar. Donor cornea should be obtained from cadaveric eyes
preferably within 6 hours, but can be permitted till 12 hrs.
Keratoplasty
Type Purpose Indications
Optical To improve vision keratoconus, scarring, corneal dystrophies
Tectonic to preserve corneal integrity descemetocele
Therapeutic facilitates removal of infected corneal Corneal ulcer
tissue
Cosmetic to improve the appearance of the eye Rarely done

Penetrating Keratoplasty:
eplacement of whole full-thickness cornea.

Lamellar Keratoplasty:
Replacement of partial thickness of cornea.
Types:
a. nlay lamellar keratoplasty – can be anterior Anterior lamellear keratoplasty or
posterior Descement Stripping Endothelial keratoplasty
b. Onlay lamellar keratoplasty – Epikeratoplasty/Epikeratophakia.

Fig.3.34: PENETRATING KERATOPLASTY

54 | Ophthalmology

Fig.3.35: LAMELLAR KERATOPLASTY (in lays)

Fig.3.36: ANTERIOR LAMELLAR KERATOPLASTY

 orn a and l ra | 55

Fig.3.37: POSTERIOR LAMELLAR KERATOPLASTY

Keratoprostheses
They are artificial corneal implants used in patients unsuitable for keratoplasty.
ndicated in bilateral blindness from severe but inactive anterior segment disease with
no realistic chance of success from conventional keratoplasty, e.g. Stevens–Johnson
syndrome, ocular cicatricial pemphigoid, chemical burns and trachoma.

Fig.3.38: Boston keratoprosthesis Fig.3.39: Osteo-odonto keratoprosthesis

56 | Ophthalmology
Concept 3.7: Sclera:
Learning objectives
ƒ To learn salient features of scleritis and episcleritis
ƒ To know about types of staphylomas

Time Required
1 reading
st
25 mins
2 look
nd
10 mins

Episeleritis Scleritis
Pathophysiology diopathic in ammation Autoimmune dysregulation
Symptoms Acute onset Mild pain Redness, Subacute onset Severe pain Pain with eye
irritation movement Blurred vision/vision loss Photophobia
Physical Exam Mobile vessels Adherent vessels
Blanch with phenylephrine drops Does NOT blanch with phenylephrine drops
Reddish hue Bluish hue
Slit lamp may reveal nodules, scleral thinning, and
corneal changes
Systemic in ammation oint pain, rashes, etc
Treatment Self-limited Ophthalmology consult
Consider topical steroids in Systemic steroids/NSAIDs +/- Topical antibiotics
refractory cases

Fig.3.40: Episcleritis Fig.3.41: Scleritis

Scleromalacia Perforans:
t is anterior necroti ing scleritis without inflammation.
Common in women with long-standing seropositive rheumatoid arthritis. Spontaneous
perforation is rare, unless intraocular pressure is elevated.
 orn a and l ra | 57
Staphyloma:
t is an ectatic condition of the eyeball with herniation of uveal tissue
Type Uveal tissue lining Cause
Anterior staphyloma Iris plastered behind Pseudocornea (the scar formed from organized
sloughed cornea exudates and fibrous tissue covered by epithelium
Intercalary staphyloma Occurs at limbus, lined Causes are secondary angle closure glaucoma,
internally by root of iris and cataract surgery, scleromalacia perforans, anterior
anterior portion of ciliary scleritis, marginal corneal ulcer and in uries to
body. limbus.
Ciliary staphyloma Ciliary body is incarcerated in Causes are scleritis, trauma, developmental
the region of sclera ectasia. glaucoma, end stage primary/secondary glaucoma.
Equatorial staphyloma Occurs at equatorial region Causes are uncontrolled glaucoma, scleritis,
of the eye with incarceration degenerative myopia.
of the choroid.
Posterior staphyloma Occurs at posterior pole and is egenerative high axial myopia is a ma or cause
lined by choroid from inside.

Fig.3.42:

Fig.3.43: Anterior Fig.3.44: Intercalary

58 | Ophthalmology

Fig.3.45: Ciliary Fig.3.46: Posterior

 orn a and l ra | 59
Worksheet
• DO TH S CHAPTE F O D B

• E T A PO NTS F O D B


60 | Ophthalmology
• ost vital layer of cornea is
• nvestigation to measure corneal thickness is
• Satellite lesions are characteristic of which corneal ulcer

hat is checked with this device

hat is the treatment of this

Name the conditions in which these lines are seen

Fleischer’s ring
Hudson-Stahli line
Stocker’s line

Ferry’s line
Siderosis

Write some important signs of keratoconus

 orn a and l ra | 61
Identify the deposit and layer of cornea involved-

Identify

Identify the procedure

62 | Ophthalmology

Fill the boxes for type of staphylomas

Fill in the remaining points

Corneal Dystrophies

Layer Dystrophy Deposit characteristics

Epithelial - subepithelial Microcystic (Cogans)(epithelial basement
membrane)
Tiny epithelial cysts.
Epithelial - stromal

Stromal Macular
Endothelial Fuch’s endothelial
Posterior polymorphous Vesicular
or band-like opacities
 orn a and l ra | 63
EXTRA POINTS:
 4 ConjunCtiva

CONCEPTS
 Concept 4.1 Basic Anatomy and histology

 Concept 4.2 Allergic Conjunctivitis

 Concept 4.3 Trachoma

 Concept 4.4 Viral conjunctivitis

 Concept 4.5 Bacterial Conjunctivitis

 Concept 4.6 Cicatricial Conjunctivitis

 Concept 4.7 Conjunctival degenerations

 on n t a
Concept 4.1: Basic Anatomy and histology
Learning objectives
• To know basic conjunctival anatomy and histology

Time Required
1 reading
st
10 mins
2 look
nd
3 mins

Parts Special point

Palpebral conjunctiva Begins from the anterior margin of the edge of the lids. 3 parts: Marginal,
Tarsal and Orbital parts
Conjunctival fornix Continuous cul- de-sac uniting the palpebral and bulbar conjunctiva
Bulbar conjunctiva Covers the anterior part of the eye ball over sclera and limbus

Fig.4.1:
 Ophthalmology

Layer Special point

Epithelium Stratified squamous non keratini ed epithelium
Adenoid layer fine connective tissue reticulum
Fibrous layer contains all the blood vessels and nerves
Goblet cells: Occurs throughout the conjunctiva. More dense on the nasal side
Melanocytes: Present in limbus, fornix, caruncle and at the site of anterior ciliary
vessels
Langerhans cells: All over conjunctiva

Epithelium

Adenoid
Layer

Substantia
Propria
Fibrous
Layer

Fig.4.2:
 on n t a
Concept 4.2: Allergic Conjunctivitis
Learning objectives
• To know important features of Vernal and Phlyctenular conjunctivitis

Time Required
1st reading 20 mins
2 look
nd
5 mins

Vernal Keratoconjunctivitis:
• Also called spring catarrh
• Bilateral condition, Type I hypersensitivity to exogenous antigen, like pollen or dust.
• It is a conjunctivitis with no follicular reaction, only papillary reaction.
• Common in ages of 4-20 years.
• More common in male children
• VKC patients have increased incidence of keratoconus.
Clinical Features: Intense ocular itching, lacrimation, photophobia, foreign body
sensation, burning, thick mucus ropy like discharge
Palpebral VKC Limbal VKC
Papillary hypertrophy most marked on superior tarsus. Limbal papillae with smooth, round surface
Papillae – become large – Cobble-stone appearance. “Horner-Trantas spots” composed predominantly
of eosinophils.

Fig.4.3: Conjunctival papillae Fig.4.4: Shield ulcer

Fig.4.5: Pseudo gerontoxon – Cupids bow

 Ophthalmology
Treatment:
• Topical steroids and topical mast-cell stabilizers i.e. sodium cromoglycate.
• New drugs: Epinastine and Olopatadine: These are both mast cell stabilizers and
antihistaminics.

Phlyctenular Keratoconjunctivitis:
• Unilateral mostly.
• Type hypersenstivity- non-specific delayed hypersensitivity reaction to
Staphylococcus (most common) or tubercular antigens
• Predominantly affects children
• Small pinkish – white nodule near the limbus, surrounded by hyperaemia called
corneal Phlycten
• Corneal involvement: Fascicular ulcer or Sacrofulous ulcer

Fig.4.6:

Treatment:
• Topical steroids.
• Any associated staphylococcal blepharitis must be treated.
 on n t a
Concept 4.3: Trachoma
Learning objectives
• To learn and identify clinical signs of trachoma and to know its management

Time Required
1st reading 20 mins
2 look
nd
5 mins

• Chronic Keratoconjunctivitis.
• By Chlamydia trachomatis – Serotypes A, B, Ba, C.
• Conjunctival reaction in trachoma is both follicular and papillary
• Chlamydia trachomatis is epitheliotropic and produces intra – cytoplasmic inclusion
bodies called H.P bodies (Halber Staedter – Prowazeke bodies)
• ajor vector of infection is flies
• Incubation period is 5-12 days
• Clinical features: 1-9 year child presents with lot of itching and watering. There are
follicles (boiled Sago grain appearance) in the upper palpebral conjunctiva and upper
limbus.
• SAFE strategy : It is a WHO strategy to control trachoma in a [Link] stands for
Surgery, Antibiotics, Facial Cleanliness, Environment.
• Treatment: The choice of treatment is Azithromycin.
• Other drugs: Tetracycline ointment 1%, Topical erythromycin eye ointment and
topical sulphonamides eye drops and ointmen

classification of t achoma nemonic S

rachomatous in ammation follicular resence of five or more
follicles with 0.5 mm in diameter in the upper tarsal conjunctiva.

Follicles
rachomatous in ammation n ammatory thickening of the
tarsal conjunctiva that obscures more than half of the normal deep
tarsal vessels
rachomatous scarring S he presence of scarring in the tarsal
conjunctiva. Arlt’s line: Linear scar in sulcus subtarsalis

Arlt’s line
rachomatous trichiasis t least one eyelash rubs on the eyeball
orneal pacity

Trichiasis and corneal opacity

 Ophthalmology

Fig.4.7: Herbert’s pits: Cicatrized follicles at the Fig.4.8: Pannus Infiltration of cornea associated with
superior limbus. vascularization
 on n t a
Concept 4.4: Viral Conjunctivitis:
Learning objectives
• To learn features of adenoviral conjunctivitis

Time Required
1st reading 10 mins
2 look
nd
5 mins

Typical viral lesion is a keratoconjunctivitis.

Causes- Adenovirus, HSV, Herpes zoster virus, Poxvirus, Myxovirus, Paramyxovirus.

Adenoviral Keratoconjunctivitis:
sually affects children with pper respiratory tract infection

Fig.4.9: Chemosis of conjunctiva

Clinical features Types

Watering, discomfort, photophobia Pharyngo conjunctival fever
Follicular response Epidemic kerato conjunctivitis
Preauricular adenopathy
Severe causes
• Subconjunctival haemorrhage
• Chemosis
• Pseudo membranes
• ocal white subepithelial anterior stromal infiltrates probably as
an immune response to the virus
Treatment – Conservative, cold compresses, topical antibiotics (to prevent secondary
infection)
 Ophthalmology
Concept 4.5: Bacterial Conjunctivitis:
Learning objectives
• To learn few examples and salient features of bacterial conjunctivitis

Time Required
1st reading 25 mins
2 look
nd
10 mins

The most common isolates are Streptococcus pneumoniae, Staphylococcus aureus

most common , Haemophilus influen ae and oraxella catarrhalis
• Acute onset of redness, grittiness, burning and discharge
• The discharge can initially be watery, mimicking viral conjunctivitis, but rapidly
becomes mucopurulent (can lead to Coloured halos sometimes)
• Hyperacute purulent discharge may signify gonococcal or meningococcal conjunctivitis,
which may have lymphadenopathy as well

Fig.4.10: Mucopurulent discharge

Treatment
Topical antibiotics
Systemic antibiotics for Haemophilus influen a, gonococcal or meningococcal
conjunctivitis
 on n t a

Conjunctivitis Organisms Treatment

Acute Membranous • Corynebacterium diptheriae Topical penicillin and topical
Conjunctivitis • Virulent type of Streptococous antidiphtheric serum
haemolyticus
Pseudomembranous Severe Adenoviral infection Topical antibiotics and anti-
Conjunctivitis Ligneous conjunctivitis. in ammatory.
(it does not bleed on Gonococcal conjunctivitis.
peeling)
Autoimmune conjunctivitis.
Streptococcus haemolyticus.
Low virulent diphtheria infection.
Chemical causes: Lime, Acids, Ammonia,
Copper sulfate.
Angular Conjunctivitis orax xenfeld diplobacilli diplobacillary Oxytetracycline- inhibits the growth of
con unctivitis organisms
ine lotion t inhibits proteolytic
en ymes.
Acute Haemorrhagic Bacterial -Pneumococcus and Haemophilus. Self–limiting – resolves in 7 days
Conjunctivitis irus icorna viruses nterovirus most
common and coxsackie . denovirus type
, chovirus
Ophthalmia hlamydial manifest after days. Prophylaxis: 0.5% eryhthromycin and 1%
Neonatorum tetracycline ointment
(conjunctival onococcal manifest after days.
in ammation that Specific treatment
Chemical: due to 1% silver nitrate given to
occu s u in the fi st
prevent gonococcal conjunctivitis- within Gonococcus: Systemic ceftriaxone,
month of life)
hours. cipro oxacin, penicillin etc.
Staphylococcus aureus –end of 1st week HSV: Acyclovir eye ointment or systemic
erpes simplex t occurs due to S Acyclovir.
manifest 1to 2 weeks Chlamydia trachomatis: eryhthromycin
eye ointment, oral erythromycin.

Fig.4.11: Membranous conjunctivitis Fig.4.12: GONOCOCCAL CONUNCTIVITIS

Fig.4.13: Hemorragic conjunctivitis

 Ophthalmology
Concept 4.6: Cicatricial Conjunctivitis:
Learning objectives
• To learn features of Keratoconjunctivitis Sicca and Xerophthalmia
• To lean few investigations for dry eyes

Time Required
1 reading
st
mins
2nd look 15 mins

P e co neal tea film has th ee la e s

ea film la e Glangs producing
Lipid layer Meibomian and Zeiss
queous layer ain lacrimal glands and accessory lacrimal glands of rause and olfring
Mucin layer oblets cells, lands of enle and an

Fig.4.14:

e atocon uncti itis Sicca S

It refers to any eye with some degree of dryness. It primarily resulting from aqueous
layer deficiency.
Sjogren syndrome is an autoimmune inflammatory disease of which dry eyes is a
feature
 on n t a
e es classifie as

Aqueous-deficient Evaporative

Sjögren
syndrome dry Non-Sjögren
Intrinsic Extrinsic
eye (primary or syndrome
secondary

on S o en s n ome e e
• acri al de cienc primary (e.g. age-related dry eye, familial dysautonomia) or
secondary e.g. inflammatory and neoplastic lacrimal gland infiltration
• Lacrimal gland duct obstruction, e.g. trachoma, cicatricial pemphigoid, chemical
injury, Stevens–Johnson syndrome

nt insic
• eibomian gland deficiency, e.g. posterior blepharitis, rosacea.
• Disorders of lid aperture, [Link] retraction, proptosis
• Low blink rate, e.g. Parkinson disease, prolonged computer monitor use, reading,
watching television.

Extrinsic
• itamin A deficiency.
• Contact lens wear.
• Allergic conjunctivitis.

n esti ations
ea film ea u time Normal – 34 seconds.
secon s a no mal
Rose Bengal Staining
Fluoroscein staining
Lissamine staining
Schirmers test Normal > 15 mm.
orderline etween mm and mm.
Abnormal - <5 mm.
Phenol red thread test

Lactoferrin level in tears t decreases in dry eye.

Tear osmolality measurements t is raised in patients of dry eye.

 Ophthalmology

Fig.4.15: CICATRICIAL CONJUNCTIVITIS Fig.4.16: PHENOL RED THREAD test

Fig.4.17: SCHIRMER test Fig.4.18: ROSE BENGAL STAINING

Treatment:
1. Tear substitutes:
a. Cellulose derivatives.
b. Polyvinyl alcohol.
2. Mucolytic Agents – 5% acetylcysteine drops.
3. Reduction of tear drainage – Punctal Occlusion.
Xerophthalmia describes a dry eye associated with vitamin A deficiency

he classification of itamin eficienc is as follo s

XN Night blindness
X1A Conjunctival xerosis
X1B Bitot's spot
X2 Corneal xerosis
X3A Corneal ulceration/keratomalada involving one-third or less of the cornea
X3B Corneal ulceration/keratomalada involving one-half or more of the cornea
XS Corneal star
XF Xerophthalmic fundus
 on n t a
P e alance fo P
Criteria P e alence in o ulation at is
Night blindness >1%
Bitot's spots >0.5%
Corneal xerosis/corneal uiceration/keratomaJacia >0.01%
Corneal ulcer >0.05%
Serum Retinol mcg dl >5%

Fig.4.19: BITOT SPOT Fig.4.20: KERATOMALACIA

Treatment:
ocal cula he ap
a. Topical artificial tears.
b. f eratomalacia – full-fledged treatment of corneal ulcer.

B. Vitamin A Therapy:
Age Oral dose at 0,1 and 14 days
< 6 months
6 m – 1 year lakh
>1 year lakh

eatment of un e l in con itions

a. Treatment of PEM – Protein Energy Malnutrition.
b. Other nutritional disorders, diarr- hoea, dehydration and electrolyte imbalance.

P oph la is of e ophthalmia
• 6-12 months – 1 lakh IU orally every 3-6 months.
• 1-6 years – 2 lakhs IU orally every 6 months.
• < 6 months – 50,000 IU orally.
• Lactating mothers – 20,000 IU orally once at delivery or during next 2 months.
 Ophthalmology
Concept 4.7: Conjunctival degenerations:
Learning objectives
• To learn about pterygium and pingencula

Time Required
1st reading 20 mins
2 look
nd
5 mins

Pterygium
• Degenerative and hyperplastic condition of conjunctiva.
• The subconjunctival tissue undergoes elastotic degeneration and proliferates as
vascularized tissue.
• Corneal epithelium, bowman’s layer and stroma is destroyed.
• Etiology: UV rays, dry heat, dusty environment.
• It appears to be a triangular fold encroaching over the cornea in the area of palpebral
aperture, usually on nasal side.
• It is an asymptomatic condition in early stages except for cosmetic intolerance.
Visual disturbance due to encroachment of pterygium on papillary area or corneal
astigmatism.
• Diplopia can very occasionally occur due to ocular movement limitation.

Treatment:
Asymptomatic is best left alone.
Otherwise surgery is the only effective treatment.
Simple excision or Bare sclera technique is associated with high recurrence (80%), so
conjunctival autografting is the most popular approach

Fig.4.21: Stocker line (iron deposition in epithelium of cornea)

Pingencula
Asymptomatic elastotic degeneration of the conjunctival
stroma. A yellow–white fatty like mound is seen on the
bulbar conjunctiva. Calcification is occasionally present.
Treatment is usually unnecessary

Fig.4.22
 on n t a
Worksheet
• DO THIS CHAPTER FROM DQB

• EXTRA POINTS FROM DQB


 Ophthalmology
• Phlyctenular Keratoconjunctivitis is which hypersensitivity reaction _____________
• Chlamydia trachomatis is caused by which serotypes ________________________
__________
Most common cause of vision deterioration in this is - ____________________________

Name some causative agents

Acute Haemorrhagic Conjunctivitis Bacterial -.
Virus -

Angular Conjunctivitis Organism? Treatment?

• Give two differentials of this

Fill in the values

Schirmers test Normal > .
orderline
Abnormal - <5

ea film la e Glangs producing

Lipid layer
queous layer
Mucin layer
Treatment for 2 year old child with this is _______________________
 on n t a

Identify the line marked by arrow - _______________

Identify the IOL - _______________

ist classification of e ophthalmia

Ophthalmology
P S
 5 Retina

CONCEPTS
 Concept 5.1 Basic Structure

 Concept 5.2 Layers of retina

 Concept 5.3 Vascular supply of retina and related

investigations

 Concept 5.4 Retinal detachment

 Concept 5.5 Diabetic Retinopathy

 Concept 5.6 Hypertensive Retinopathy

 Concept 5.7 Retinal vein occlusions

 Concept 5.8 Retinal artery occlusions

 Concept 5.9 Retinal degenerations

 Concept 5.10 Retinal dystrophy

 Concept 5.11 Retinopathy of Prematurity

84 | Ophthalmology
Concept 5.1: Basic Structure
Learning objectives
• To know basic retinal structure and parts

Time Required
1st reading 15 mins
2 look
nd
5 mins

• Retina extends from optic disc (thickest) to ora serrata (thinnest)

• Ora serrata corresponds to the insertion of the rectus muscles. Its thickness is 0.10
mm
• The surface area of the retina is 266 mm2

Fig.5.1:

Diameter isual fiel

Optic disc 1.5 mm Blind spot Vertically oval,
1.76 mm horizontally and 1.88 mm vertically.
Macula 5.5 mm 15° Contains xanthophyll
carotenoid pigments lutein and zeaxanthin in
higher concentration
than the peripheral retina
Fovea- Centralis 1.85 mm 5° depression at the centre of macula
Foveola 0.35 mm 1° 2 disc dioptre away from temporal margin of optic
disc
• mbo- tiny depression at centre of foveola. Seen as foveal reflex.
• FAZ- (Foveal Avascular Zone): It doesn’t contain any capillaries, hence the name.
nside the fovea but outside foveolar. determined with accuracy only by fluorescein
angiography (0.8 mm diameter)
 t na | 85
Concept 5.2: Layers of retina
Learning objectives
• To know and identify retinal layers

Time Required
1st reading 20 mins
2 look
nd
5 mins

RETINA HISTOLOGY

Fig.5.2:

erve fiber layer nner limited membrane

Axons at surface of retina
passing via optic nerve,
8 Ganglion cell layer chiasm and tract to lateral
geniculate body

7 Inner plexiform layer Ganglion cell

Muller cell
6 Inner nuclear layer (supporting glial cell)
Bipolar cell

Amarcine cell
5 Outer plexiform layer
Horizontal cell
Rod
Cone
4 Outer nuclear layer
3 Outer limiting
membrane Pigment cells
2 Photoreceptor layer

1. Pigment epithelium
Choroid

Fig.5.3:
86 | Ophthalmology

Layer
nternal limiting membrane
erve fibre layer Axons of ganglion
cells running centrally into the optic nerve
Ganglion cell layer
Inner plexiform layer consisting of synapses
Inner nuclear layer the nuclei of the bipolar, uller, amacrine, hori ontal cells
Outer plexiform layer consisting of synapses
Outer nuclear layer the nuclei
of the rods and cones
xternal limiting membrane
Photoreceptors This layer transform light energy to the visual impulse. There are
120 million rod cells and 6 million cone cells
Retinal Pigment Epithelium exagonal cells, firmaly adherent to bruch s membrane and
loosely to rods and cones of the sensory retina. This layer provide
metabolic support to neuro sensory layer. ther important
fuctions are photoreceptor renewal, integrity of subretinal space,
phagocytic of photoreceptor, regenerative and reparative
Most radiosensitive layer of the retina: Rods and cones.
Most radioresistant layer of the retina: Ganglion cell layer.

Fig.5.4: NORMAL Optical Coherence Tomography

 t na | 87
Concept 5.3: Vascular supply of retina and related investigations
Learning objectives
• To learn blood supply of retina
• To learn about angiography

Time Required
1 reading
st
20 mins
2nd look 10 mins

Retinal vascular system Inner six layers derive its nutrition from central retinal artery. The retinal
vessels are end arteries and do not anastomose with each other.
ho oi al ascula s stem Outer four layers of retina get its nutrition from choriocapillaries i.e.
choroidal vascular system (short posterior ciliary artery)
There is anastomosis of central retinal artery and short posterior artery with the arterial
circle of Zinn or Haller.

Blood supply of optic nerve head/optic disc.

• Surface nerve fibre layer: Derived from retinal arterioles
• Prelaminar region: Vessels of ciliary region.
• Lamina cribrosa: Short post ciliary artery and circle of Zinn.
• Retrolaminar region: Both ciliary and retinal circulation.

Blood-Retinal Barrier:
• Inner: Tight junctions of retinal capillary endothelial cells.
• Outer: Retinal pigment epithelial cells.
Arteriole Venule
Inner limiting membrance

Superficial
capillary etinal nerve fibre layer
network

Ganflion cell layer

Ineer plexiform layer

Deep
capillary Ineer nuclear layer
network

Outer plexiform layer

Outer nuclear layer

Outer limiting
membrance
Rod and cone layer

Pigment epithelium

Fig.5.5:
88 | Ophthalmology
Fluorescein Angiography (FA):
FA is used in studying the normal physiology of the retinal and choroidal circulation and
to detect any abnormalities.
Procedure:
5 ml of 10% Fc is injected in antecubital vein and photograph taken at 1sec interval
between 5 and 25 s after injection.

Findings:
t may be normal, hypoflourescence or hyperflourescence.
po ourescence: t may be due to blocked fluorescence as a result of haemorrhage
or exudates OR due Capillary Non-Perfusion.
per ourescence: It occurs either due to leakage or RPE defects. A leakage will
increase in size but size of RPE defects will remain normal.
Indocyanine Angiography:
ICG angiography is helpful for diagnosing choroidal lesions as it is 98% bound to the
plasma proteins.

Fig.5.6: NORMAL ANGIOGRAPHY

 t na | 89
Concept 5.4: Retinal Detachment
Learning objectives
• To learn about different types of detachment
• To learn about Central Serous Retinopathy

Time Required
1 reading
st
35 mins
2nd look 15 mins

Separation of sensory retina from retinal pigment epithelium PE by subretinal fluid.

Type of Patholo an Features onfi u ation Treatment
etachment cause
Rhegmatogenous ue to break • Floaters: opacities Convex Vitreo-retinal
formation in the vitreous surgery
either due to cavity (Pars plana
traction, trauma • hotopsia ash of vitectomy)
or predisposing light seen by the or
degenerations. patient. It occurs Scleral buckling
due to irritation of
rods and cones.
• Decreased visual
acuity if macula is
involved.
• isual field defect

obility etached
retina undulates
freely.
Tractional Vascular • Decreased visual Concave Vitreo-retinal
pathology of acuity if macula surgery
retina like DM, is involved. (Pars plana
CRVO, Eales • isual field defect vitectomy)
disease • obility
Reduced
Exudative Due to choroidal • Floaters: They Convex Treatment of the
lesions like are seen due to primary choroidal
tumour associated vitritis. lesions
[Melanoma, • Vision
Hemangioma or diminuition
metastasis] or is sudden and
Central Serous progresses rapidly
Retinopathy • Smooth retina
• Shifting uid
Present
90 | Ophthalmology
Grey reflex: in old detached retina on distant direct ophthalmoscopy
Vitreous substitutes that can be used are Air, SF6, perflourocarbons like C F and
silicone oil.
Scleral buckling - Aim of treatment in rhegmatogenous D is closure of break.
a. Drainage of S F subretinal fluid .
b. Injection into vitreous: To repose the detached retina:
c. Cryotherapy: To seal retinal break
d. Explant: Buckling is done to internally indent the sealed break. It is done with buckle
explant or encirclage band

RETINAL DETACHMENT

Fig.5.7: PARS PLANA VITRECTOMY(PPV)

Fig.5.8: SCLERAL BUCKILING

 t na | 91

Fig.5.9: SILICONE OIL IN ANTERIOR CHAMBER

Central Serous Retinopathy (CSR):

Idiopathic, self-limited disease of young or middle –aged adult males (20-40 years).

Pathogenesis:
Dysfunction of PE
↓
Accumulation of fluid in subretinal space
↓
Local detachment of sensory retina at macula
Clinical features
Sudden onset of blurred vision painless
Micropsia
Metamorphopsia
is mild vision loss
levation of sensory retina at posterior pole, borders of which are outlined by glistening re ex Ring Re ex

Fig.5.10: CENTRAL SEROUS RETINOPATHY Fig.5.11: INK BLOT/SMOKE STACK IN CSR

Treatment:
• Spontaneous resolution is common (by 6-12 months).
• Laser photocoagulation – hasten symptomatic relief by speeder resolution of serous
detachment.
92 | Ophthalmology
Concept 5.5: Diabetic Retinopathy
Learning objectives
• To learn about different types of detachment
• To learn about Central Serous Retinopathy
• To learn about Cystoid macular edema

Time Required
1 reading
st
60 mins
2 look
nd
20 mins

Prevalence of D is higher in DDs 5 years than in N DDs can present with D at

time of diagnosis).

Risk Factors for DR:

• Duration of diabetes: ost important factor.
• Good metabolic control: Delays the development of D by few years.
• Miscellaneous Factors: Pregnancy, anaemia, hypertension, renal disease.
t’s a microangiopathy affecting the retinal precapillary arterioles, capillaries and venules.
Pathogenesis:
• Aldose reductase reduces glucose to sorbitol resulting in its accumulation which further
results in activation of protein kinase C,oxidative stress and increased production of
growth factors EGF-A, GF, EGF, PDGF, TGF-B .
• The above said factors lead to the endothelial and metabolic dysfunction which lead
to microangiopathy and features of diabetic retinopathy.

Features of DR
Non-Proliferative DR Proliferative DR
icroaneurysm irst clinically detectable lesion of eovascularisation , , Rubeosis iridis
DR (Inner nuclear layer) NVG
ntra retinal aemorrhage ot and blot deep RD: Tractional RD can later lead to Rhegmatogenous
ame shaped superficial . RD
Hard exudates: Lipid deposits within the retina Haemorrhage: intravitreal, pre-retinal
Soft exudates cotton wool spots ue to disturbance
of axoplasmic ow which causes accumulation of
waste product in nerve fibre layer
enous looping, beading and sausage like
segmentation.
R intra retinal microvascular abnormalities .
A-V shunts due to capillary closure.
 t na | 93
lassification of
a e Features
No DR o abnormality
Mild NPDR Microaneurysm a only
Moderate NPDR More than just microaneurysms and less than severe NPDR
Severe No signs of PDR
NPDR Presence of any one of the following
4 quadrants of intra retinal hemorrhages
(> 20/quadi ant)
enous beading in quadrants
IRMA in >1 quadrant
PDR Presence of neovascularization
Presence of preretinal or vitreous hemorrhage

Follow up for mild/moderate NPDR

Treatment of severe NPDR: Strict follow-up to watch for changes of PD . Consider
PRP in high risk cases
Treatment of PDR: PRP- Pan-retinal photocoagulation.
Pars plana vitrectomy: when D or persistent vitreous haemorrhage
Few Studies Done in D :
• D S: Diabetic retinopathy study.
• ETD S: Early treatment diabetic retinopathy study.
• D S: Diabetic retinopathy vitrectomy study

Fig.5.12: MICRO-ANEURYSMS Fig.5.13: NON-PROLIFERATIVE RETINOPATHY

94 | Ophthalmology

Fig.5.14: Fig.5.15:

Fig.5.16: PROLIFERATIVE DR Fig.5.17: PAN-RETINAL PHOTOCOAGULATION

Cystoid Macular Edema (CME):

Accumulation of fluid in the outer plexiform Henle’s and inner nuclear layers of the
retina, centred about the foveola
Etiology of CME Treatment

Ischemia R , iabetic retinopathy Anti VEGF intravitreally /Laser photocoagulation

n ammation uveitis, post operative CME) Steroids

Drugs Epinephrine in aphakia, latanoprost Stop drugs

and betaxolol

Mechanical vitreous traction on macula Vitrectomy

Heredity retinitis pigmentosa, inherited Systemic carbonic anhydrase inhibitors

CME

linicall si ni cant acular oede a N D ABET C ET NOPATH

t is detected on clinical examination as defined in the ETD S
 t na | 95

Retinal thickening within 500 µm of the centre of the macula

Exudates within 500 µm of the centre of the macula, if associated with retinal thickening
Retinal thickening one disc area (1500 µm) or larger, any part of which is within one disc diameter of the
centre of the macula

Treatment: aser photocoagulation anti in ections intravitreally

Fig.5.18: CME on OCT

Fig.5.19: Flower petal appearance on Angiography

96 | Ophthalmology
Concept 5.6: Hypertensive Retinopathy
Learning objectives
• To learn grading and signs of Hypertensive retinopathy

Time Required
1st reading 15 mins
2 look
nd
5 mins

Keith –Wagner Grading:

a e il to o e ate ene alise a te iola attenuation
Grade II • Moderate-to-Marked narrowing of arterioles.
• Generalised and focal narrowing of arterioles.
• Salus sign de ection at crossing
Grade III • onnet sign banking of veins , unn s sign tapering of veins on either side of the
crossing).
• aemorrhages superficial or ame shaped .
• Cotton wool patches.
• Retinal edema
Grade IV Grade III changes + silver wiring of arterioles + disc swelling
apilledema acular star appearance
Other Ocular Manifestations of Hypertension:
• Subconjunctival haemorrhage.
• Retinal vein occlusion
• Elschnig’s spots- ischemic choroidal infarcts.
• Macroaneurysms.
• schemic optic neuropathy Non-Arteritic A ON .
• Ocular motor nerve palsies

Fig.5.20: Macular star appearance in Grade 4

 t na | 97
Concept 5.7: Retinal vein occlusions
Learning objectives
• To learn and identify features of Retinal Vein Occlusions

Time Required
1st reading 20 mins
2 look
nd
5 mins

Predisposing factors:
• Increasing age – 6th/7th decade.
• Unilateral.
• Systemic hypertension, Diabetic mellitus, Arteriosclerosis.
• Blood dyscrasias – Hyperviscosity
• Raised IOP.
• Hypermetropia
• Periphlebitis – Sarcoidosis, Behcet’s disease.
• Use of OCPs

Clinical features:
• Decreased visual acuity.
• oss of part of the visual field.
• Dilated and tortuous veins, flame- shaped and deep haemorrhages. etinal edema,
cotton-wool spots.

Complications:
• CME
• Neovascularisation leads to vitreous haemorrhage and T D

Fig.5.21: Central Retinal Vein Occlusion Fig.5.22: Branch Vein Occlusion

98 | Ophthalmology

Non-ischemic CRVO schemic

Frequency 75-80% 20-25%
Visual acuity Better than 6/60 Worse than 6/60
RAPD Slight or nil Marked
isual field defect Rare Common
Fundus Less hemorrhages and cotton wool spots Extensive hemorrhages and cotton wool spots
FFA Good perfusion Non-perfusion > 10DD
ERG Normal Reduced b wave amplitude
Prognosis , or better Rubeosis or
Splashed sauce appearance: ultiple flame-shaped haemorrhages around disc in
ischemic CRVO
100-day glaucoma: Neovascular glaucoma in ischemic CRVO is seen to occur after
100 days of occlusion hence the name.
Treatment: CRVO – PRP, BRVO - Scatter laser photocoagulation
 t na | 99
Concept 5.8: Retinal artery occlusions
Learning objectives
• To learn and identify features of Retinal artery Occlusions

Time Required
1st reading 20 mins
2 look
nd
5 mins

Central etinal Artery Occlusion: Due to emboli from atherosclerosis from heart or
carotid artery

Fig.5.23:

Clinical features:
• Acute and profound, PAINLESS loss of vision.
• White cloudy/milky white retina due to intracellular edema- Cherry-red spot
• Marcus - Gunn pupil
• Segmentation of blood column in venules and arterioles: Cattle –Track Appearance
of blood flow.

Treatment: Ocular emergency:

• Lower IOP - Firm ocular massage/Intravenous acetazolamide –500 mg.
• Inhalation of carbogen i.e. a mixture of 5% CO2 and 95% of O2.
• Anterior chamber paracentesis.
• Alteplase or tPA can be given.
i e ent ia nosis o
SPOT:
1. CRAO
2. Tay sachs disease (GM1 Gangliosidosis –
type I)
. Niemann-pick disease.
4. GM1 Gangliosidosis – type I
5. Sialidosis
6. Berlins edema.
Fig.5.24: CRAO with cilio-retinal artery
7. Gaucher disease
sparing (Central retina is spared)
100 | Ophthalmology
Concept 5.9: Retinal Degenerations
Learning objectives
• To learn names and features of various retinal degenerations
• To learn about features of Age- elated acular Degeneration

Time Required
1 reading
st
25 mins
2nd look 10 mins

Predisposing Vitreo-Retinal Degenerations to Retinal Detachment

Latttice Degenerations Common in high myopes
Circumferentially oriented, spindle- shaped areas of
retinal thinning
ay be associated with holes or retinal tears

Snail-track Denegerations
Acquired retinoschisis
White with pressure
White without pressure

Myopic Maculopathy degeneration

Annular crescent / temporal crescent surrounding optic disc
acquer cracks can lead to choroidal neovascularisation. hese are cracks in the bruch s membrane can
have holes break
Rhegmatogenous RD
uchs spots uch s ecks aemorrhage and pigment accumulation in the macula.
Chorioretinal atrophy at posterior pole
Macular holes
Posterior staphyloma.

Age-Related Macular Degeneration (ARMD)

t is a degenerative disorder affecting the macula in old age
 t na | 101
Types of ARMD
on e u ati e u ati e et
ost common of cases 10% of the cases
Gradual, mild to moderate impairment of vision over Visual impairment is within days and may lead to
months or years loss of all central vision

Drusens Choroidal neovascularisation

RPE atrophy eakage of uid
RPE detachment. RPE detachment

o effective treatment. s below

• Low visual aids
• Antioxidants
• Vitamin E (400 IU)
• Vitamin C (500 mg)
• Lutein (10 mg).
• Zeaxanthin (2 mg).
• inc mg
• Copper (2 mg)

Fig.5.25: Drusens in Dry ARMD Fig.5.26:

Treatment of Wet ARMD

Extrafoveal more than 200 µm from centre of FAZ (foveal Laser photocoagulation
avascular zone)
Juxtafoveal ot involving centre but closer than m. Laser photocoagulation/ PDT
(Photodynamic therapy)
Subfoveal Involving centre of FAZ PDT
Anti-VEGF agents: All CN subtypes respond to anti- EGF therapy, but benefit is only
likely in the presence of active disease They inhibit the growth of new blood vessels.
They are:
Aflibercept Eylea , anibi umab ucentis , Bevaci umab Avastin , Pegaptanib
(Macugen)
102 | Ophthalmology
PDT – It relies on photochemical injury to the vessel wall and selective damage to the
target tissue while sparing the adjacent normal tissue.
PDT requires two components:
• Photo sensiti er –Commonly used is Ben oporphyrin derivative – erteporfin.
• A specific laser light corresponding to the absorption peak of the dye 6 0nm

Choroidal Neovascularisation:
Proliferation of fibrovascular tissue from choriocapillaris through defects in Bruch’s
membrane into sub- RPE space and later into the sub –retinal space.
Cuses of Choroidal Neovascularisation
Wet ARMD
POHS – Presumed Ocular Hstoplasmosis syndrome.
Severe myopia.
Angioid streaks
Choroidal rupture
Inappropriate laser photocoagulation.
Optic disc drusen.
 t na | 103
Concept 5.10: Retinal Dystrophy
Learning objectives
• To learn names and corresponding layers of various retinal dystrophies
• To learn about features of Retinitis pigmentosa
• To learn about Electroretinogram and Elecrooculogram

Time Required
1st reading 40 mins
2 look
nd
15 mins

Retinitis Pigmentosa:
It’s a photoreceptor dystrophy with damage to rod system is predominant

Sporadic Most common

AD Most common mode of inheritance
Best prognosis
X-linked recessive Worst prognosis and least common

Clinical features:
• Nyctalopia/night blindness-due to impaired rod function.
• Impaired dark adaptation.
• Tunnel vision in later stages

Classical Triad of signs:

• Arteriolar attenuation.
• Retinal bone-spicule pigmentation: These changes are perivascular
• Pale, waxy disc (consecutive optic atrophy)

Fig.5.27:

Investigations:
Subnormal amplitude of ERG mainly scotopic. EOG is also subnormal in later stages
Perimetry: In initial stage of the disease there is ring scotoma due to involvement of the
midperipheral retina whereas in the late stage patient has tubular vision.
104 | Ophthalmology
Treatment: No effective treatment
itamin A and Docosahexonoic acid can be given

Atypical Retinitis Pigmentosa:

• Retinitis punctata albescens: White dots instead of bony spicules.
• Sector RP: One sector of the retina is involved
• Pericentric P: Disease starts from the centre
• Retinitis pigmentosa sine pigmento: Salt and pepper picture instead of bony spicule
Ocular associations of RP
stoi macula e ema
Open angle glaucoma
PSC: Posterior subcapsular cataract
Keratoconus
Myopia
isc usen

Systemic associations of RP
she s s n ome P ith ea ness t is the most common
e sum s s n ome
assen o n ei s n ome
ea ns sa e s n ome associate ith ocula m o ath an hea t e ects
a et ie l s n ome mental han ica ol act l
au ence oon s n ome eatu es o a et ie l s n ome ith s astic a a le ia
oc a nes s n ome
ie eich s ata ia

Best vitelliform and Stargardt dystrophy

est itelli o m isease ta a t isease
AD AR
Signs > Symptoms Symptoms > Signs
accumulation o li o uscin ithin the P e accumulation o li o uscin ithin the P
yolk appearance beaten-bronze aapearence
ate sta es sc am le e a ea ance
sho s co es on in h o uo escence ue to a cho oi ue to mas in
mas in o ac oun cho oi al uo escence
uto uo oscence h e auto uo escent lesion in uto uo oscence h e auto uo escent ec s
center of retina
is se e el su no mal u in all sta es EOG is commonly subnormal
 t na | 105
Treatment: No effective treatment

Fig.5.28: BEST DISEASE –egg yolk stage Fig.5.29: BEST DISEASE –scrambled egg stage

Fig.5.30: AUTO LUOROS EN E in Stargardts showing h per uoroscence

Angioid Streaks
These are crack-like dehiscences in the collagenous and elastic portions of the bruch’s
membrane with secondary changes in RPE and choriocapillaris.

Fig.5.31:
106 | Ophthalmology
It can be idiopathic or is associated with:
Pseudoxanthoma elasticum.
aget s disease.
Ehler-Danlos syndrome
Sickle cell anemia
Incontinenta pigmenti

Congenital stationary night blindness (CSNB)

• With normal appearing fundus
• CSNB with abnormal looking fundus
ƒ Fundus albipunctatus
ƒ Oguchi’s disease - Patients demonstrate Mizuo’s phenomenon (retina exhibits
yellow sheen with light exposure, which disappears with dark adaptation)

i e ential ia nosis of i ht lin ness

1. Retinitis Pigmentosa
2. Xerophthalmia.
. Congenital stationary night blindness
5. High myopia.
6. Advanced case of Primary open angle glaucoma

Bull’s Eye Maculopathy:

Central foveolar hyperpigmentation surrounded by depigmented zone and encircled by
a hyperpigmented ring. There is moderate reduction in VA- 6/18 to 6/24.

Causes:
• Chloroquine toxicity
• Cone dystrophy
• Battens disease/Batten-Mayo syndrome: It is a cerbromacular degeneration

Electrophysiological Tests:
Electroretinogram[ERG] t is the record of the action potential produced by the retina when it
is stimulated by the light of adequate intensity. t is elicited both in
photopic and scotopic state
A wave- due to rods/cones
wave due to bipolar muller cells
c- due to RPE
Electrooculogram[EOG t measures the standing action potential between the cornea
and the back of the eye. t re ects the activity of the R and the
photoreceptors [eg BEST”S Ds].
Visual Evoked Potential When light falls on the retina, the series of nerve impulses generated
and passed into the visual cortex is measured by . t indicates
activity from ganglion cell layer to the visual cortex.
 t na | 107
Concept 5.11: Retinopathy of Prematurity
Learning objectives
• To learn risk factors, staging and treatment of ROP

Time Required
1st reading 30 mins
2 look
nd
15 mins

t is a proliferative retinopathy which affects pre-term infants exposed to high ambient

oxygen concentrations. Incompletely vascularized temporal retina is particularly
susceptible to oxygen damage.

Risk factors:
• Prematurity: Gestational age 2 weeks most important
• Birth weight <1.5kg.
• Oxygen therapy: Excessive oxygen use

Pathogenesis:
Excessive free radicals
↓
Inhibit spindle cell migration
↓
Produces angiogenic factors
↓
ROP
ta e Demarcation line
ta e Ridge formation
ta e Ridge with extra retinal fibrovascular proliferation
ta e Sub total ractional Retinal etachment
Stage V Total retinal detachment.
108 | Ophthalmology

Vascularized retina Isolated neovascular tufts

Demarcation line Ridge

Severe
extraretinal Detached retina
fibrovascular
proliferation

Fig.5.32:

Fig.5.33: Zones of ROP

 t na | 109
Screening of ROP:
The most useful time is between 2 weeks and 6 weeks post conception. After 6
weeks, ROP rarely develops.
Before 2 weeks – screening after 2- weeks of birth
After 28 weeks – screening after 4 weeks of birth
Early Treatment of Retinopathy of Prematurity (ETROP)
lassification
Type 1 ROP should be treated:
one any stage of OP with plus disease one Stage OP with or without plus
disease one Stage 2 or OP with plus disease

Type 2 should be observed, and only undergo treatment if it progresses

to type I or threshold disease:
Zone II Stage 1 or 2 ROP without plus disease
one Stage OP without plus disease

ROP is treated immediately if disease is threshold disease which is:

Stage –III disease
involving Zone 1 and 2 Location
-5 contiguous clock hours or 8 noncontiguous clock hours with plus Disease.
lus isease in ol es arteriolar and enous dilatation

Treatment of ROP:
• Ablation of avascular immature retina by either cryotherapy or laser photocoagulation.
• Vitamin – E therapy – Its antioxidant role helps in prevention of the ROP.
• If Retinal detachment present Vitreoretinal surgery
110 | Ophthalmology
Worksheet
• DO TH S CHAPTE F O D B

• E T A PO NTS F O D B


 t na | 111
• Identify the cell marked _____________

• This is seen after which surgery? _______________________

112 | Ophthalmology
• Identify the sign and stage of diabetic retinopathy? ____________________

• Fill in for severe NPDR

a e Features
No DR o abnormality
Mild NPDR Microaneurysm a only
Moderate NPDR More than just microaneurysms and less than severe NPDR
Severe
NPDR

PDR Presence of neovascularization

Presence of preretinal or vitreous hemorrhage

• What is the treatment of this if its due to diabetic retinopathy? _________________

 t na | 113
• Fill in the blank spaces
Non-ischemic CRVO schemic
Frequency 75-80% 20-25%
Visual acuity Better than 6/60 Worse than 6/60
RAPD
isual field defect Rare Common
Fundus
FFA Good perfusion Non-perfusion > 10DD
ERG Normal Reduced b wave amplitude
Prognosis , or better Rubeosis or
• Write some D/D of cherry red spot

Identify the deposit and diagnosis- _______________

114 | Ophthalmology
Classical Triad of signs of this are:

- _______________ , ______________ , ______________

Identify the layer having this pathology - _______________

Fill in the remaining stages

ta e
ta e
ta e Ridge with extra retinal fibrovascular proliferation
ta e Sub total ractional Retinal etachment
Stage V
 t na | 115
Fill in the remaining points
Early Treatment of Retinopathy of Prematurity (ETROP)
lassification
Type 1 ROP should be treated:

Type 2 should be observed, and only undergo treatment if it progresses

to type I or threshold disease:
Zone II Stage 1 or 2 ROP without plus disease
one Stage OP without plus disease
116 | Ophthalmology
EXTRA POINTS:
 6 Neurophthalmology

CONCEPTS
 Concept 6.1 Visual pathway and its lesions

 oncept upillar re e

 Concept 6.3 Optic neuritis

 Concept 6.4 Papilledema

 Concept 6.5 Optic atrophy

 Concept 6.6 Supranuclear Disorder of Eye

Movement

 Concept 6.7 Nystagmus

118 | Ophthalmology
Concept 6.1: Visual pathway and its lesions
Learning objectives
• To learn about visual pathway and identify various visual field defects in lesion of
structures involved in it

Time Required
1 reading
st
40 mins
2 look
nd
15 mins

Fields of vision

Nasal
hemiretinas
Total blindness
Temporal of pslateral eye
hemiretinas
Bitemporal
Optic heteronymous
tract hemianopsia

Loop of Ipsilateral nasal

Archambault hemianopsia
(Meyer) Contralateral
homonymous
hemianopsia
Contralateral
lower quadrantie
anopsia
Contralateral
Optic
upper quadrantie
radiation anopsia
Contralateral
homonymous
Cuneus Lingual hemianopia
Callcarine with macular sparing
gyrus
sulcus
Fig.6.1:
 rophthalmology | 119

Lesion isual fiel e ects

Optic Nerve Ipsilateral blindness
Chiasma Bitemporal hemianopia. It is a heteronymous hemianopia

Anterior junction syndrome (Junctional will lead to ipsilateral central scotoma and contralateral
scotoma of Traquair: Lesion at the junction of superotemporal quandrantopia.
the chiasma and the optic nerve)
Optic Tract Incongruous homonymous hemianopia
Wernicke’s hemianopic pupil
Optic atrophy
ateral geniculate body upillary re ex Homonymous key hole defects
normal)
ptic Radiations upillary re ex normal Congruous homonymous defects
• Lesions of Temporal Radiations C/L homonymous Superior quadrantopia (Pie in sky)
• Lesions of Parietal Radiations homonymous nferior quadrantopia ie on the oor
ccipital ortex upillary re ex normal
• Occlusion of posterior cerebral artery Macula sparing congruous homonymous hemianopia
• Occlusion of middle cerebral artery Congruous homonymous macular defects

Chiasma lesions

Fig.6.2:
120 | Ophthalmology
oncept Pupilla e e
Learning objectives
• To learn about pupillary pathway and abnormal pupils
• To learn about sympathetic pathway and Horner syndrome

Time Required
1st reading 40 mins
2 look
nd
15 mins

Fig.6.3: LI T RE LE Pupillar Paras pathetic pathwa a erent nd

ner e, e erent rd ner e

Abnormal pupil reactions

a cus unn Pu il Relative fferent upillary efect R n Retrobulbar neuritis.

P otal fferent upillary efect n ptic atrophy.

l o e tson Pu il ight re ex absent but near re ex present.

olmes ie Pu il onic pupil with slow response to light and near. ue to denervation of post
ganglionic supply.

o ne s n ome ue to disruption of sympathetic pathway. haracterised by ptosis, miosis same

in dark conditions , enophthalmos. upillary reaction to both light and near are
normal. Heterochromia iridis in congenital cases.
 rophthalmology | 121

Fig.6.4: RELATIVE AFFERENT PUPILLARY DEFECT (RAPD)

122 | Ophthalmology

Fig.6.5: ARGYLL –ROBERSTON PUPIL

Fig.6.6: HOLMES –ADIE PUPIL

 rophthalmology | 123

Fig.6.7: S pathetic pathwa entral (fro h pothala us to T ), Pre ganglionic till superior cer ical
ganglion, Post ganglionic to iris dilator uscle

Fig.6.8: HORNER’S SYNDROME

124 | Ophthalmology
Concept 6.3: Optic neuritis
Learning objectives
• To learn about parts of optic nerve
• To learn about various causes of optic neuritis

Time Required
1 reading
st
50 mins
2nd look 20 mins

Optic nerve
t is .5 cm to 5.5 cm long from optic disc to chiasma. t is divided into
intraocular (1 mm)
intraorbital (25-30mm)
intracanalicular (6-9 mm)
intracranial (10 mm)

Clinical Features of Optic Nerve Disease:

• Diminished visual acuity
• isual field defects - mpaired central vision most common field defect is central or
centrocecal scotoma and defective contrast sensitivity.
• Diminished pupillary light reactions i.e. APD Afferent Pupillary defect .
• mpairment of color vision
• Diminished light brightness sensitivity
• Near reflex is intact in unilateral optic nerve involvement
i ola cells 1st order neuron
tic ne e nd order neuron made up of xons of ganglion cells, . million axons are there
ate al eniculate o 3rd order neuron

OPTIC NEURITIS
Optic neuritis is an acute inflammatory optic nerve disease.

Fig.6.9:
 rophthalmology | 125
It can be divided into:
et o ul a neu itis he fundus examination is normal as the affected part of the optic nerve is behind
the eye ball
Pa illitis in ammation of optic nerve head
eu o etinitis in ammation of optic nerve and nerve fibre layer of retina.

Etiology of optic neuritis:

io athic
schemic Arteritic and non-arteritic AION
i al in ections hooping cough, measles, mumps, varicella oster.
em elinatin iso e s ultiple sclerosis, evic s disease
eta olic ut itional eficienc itamin deficiency, itamin deficiency, itamin deficiency,
olic acid deficiency, iabetes ellitus
e e ita Leber’s hereditary optic neuropathy
n ections yme s disease, syphilis, cat scratch, cryptococcal meningitis in
S,
o ic am l o ia See later
ost common cause of optic neuritis is Multiple sclerosis
• Painful eye movements seen in upward and medial direction due to attachment of a
few fibres of superior rectus and medial rectus to the durameter of optic nerve.
• hthoff sign worsening of symptoms with exercise or increase in body temperature
and Pulfrich phenomenon altered perception of moving objects .
• isual evoked response shows reduced amplitude and delayed transmission time.
• Treatment - steroids days methylprednisolone 1g/day plus 11 days of oral
prednisolone 1mg/kg/day

Lebers heredity optic neuritis

Maternal Mitochondrial DNA mutations
Clinical features:
ƒ Typically in males - third decade.
ƒ Initially unilateral visual loss, fellow eye involved within 2 months.
ƒ Bilateral optic atrophy
ƒ Pupillary reactions to light often remain fairly brisk

Signs:
ƒ Dise hyperemia and dilated capillaries telangiectatic microangiopathy .
ƒ ascular tortuosity.
ƒ Swelling of peripapillary nerve fibre layer
126 | Ophthalmology

Fig.6.10:

Treatment:
Prognosis is relatively poor with generally severe, bilateral and permanent visual loss.
• High–dose systemic steroids are used in some cases.
• Stop smoking and excessive drinking.

Anterior ischemic optic neuritis

t occurs due to infarction of the short posterior ciliary arteries. t is of two types-
arteritic and non-arteritic.
te itic on te itic
In patients of giant cell arteritis Unknown but the major risk factor is hypertension
Sudden loss of vision with associated headaches, Sudden painless loss of vision, mostly in morning
maurosis fugax

Visual acuity markedly reduced Slightly decreased visual acuity

Swollen optic disc. Sectoral or diffuse edema of the disc. ptic nerve
• Flame-shaped haemorrhages around the disc head is either pale or hyperaemic. lame shaped
haemorrhages around the disc.
Associated symptoms- Frontal or occipi- tal
headache with scalp tenderness, aw claudication
and polymyalgia rheumat- ica.
steroids ydrocortisone for days alongwith Treatment:
oral prednisolone which is tapered gradually • o check for viscosity affecting factors like
fibrinogen and which could be responsible
for the ischemia.
• Manage the BP.
• Manage the underlying disease.
• To stop smoking.
 rophthalmology | 127

Fig.6.11: Arteritic ische ic optic neuritis Fig.6.12: Non Arteritic ische ic optic neuritis

Pseudo - Foster- Kennedy Syndrome: in NA ON

Foster- ennedy Syndrome:
psilateral optic atrophy with contralateral papilloedema. t occurs due to tumor in orbital
surface of frontal lobe, olfactory groove or pituitary body.
128 | Ophthalmology
Concept 6.4: Papilledema
Learning objectives
• To learn about stages of papilledema
• To learn about pseudotumour cerebri

Time Required
1 reading
st
20 mins
2nd look mins

Papilloedema
Papilledema is bilateral optic nerve head swelling secondary to raised intracranial
pressure
ncreased CSF pressure
↓
Due to disturbance of pressure gradient across the lamina cribosa.
↓
Stasis of axoplasm in prelaminar area
↓
Axonal swelling
↓
enous congestion
↓
Extra-cellular edema

Fig.6.13:
 rophthalmology | 129

ta e Early sta lishe h onic t o hic

Visual acuity (VA) VA normal • Transient visual VA impaired VA severely

isturbances Constricted VF impaired
• VA normal or
impaired
• Enlarged blind
spot

Optic disc vascular • Hyperemia of • Venous tortuosity

changes margins and dilation
• Loss of • Peripapillary
spontaneous ame shaped
venous hemorrhage
pulsation • Cotton wool spots
(absent in 20% • ard exudates
of normal
individuals)

Optic disc Blurring of • Elevated disc “Champagne Secondary optic

mechanical changes margins (superior • Obliteration of cork” appearance atrophy
and inferior cup Optociliary
margin first • Retinal/choroidal shunts
folds

Treatment: According to the cause

Pseudotumour Cerebri:
Also known as Benign ntracranial Hypertension
is acto s linical eatu es n esti ations eatment

Obesity. • Headache. • scan o • iet and lifestyle

OCPs. • B/L disc edema neurological lesion. Weight loss.
Hypervitaminosis A. • or sixth • Increased CSF • Carbonic anhydrase
Tetracycline nerve palsy leads to pressure. inhibitors i.e.
diplopia. • Normal CSF ceta olamide
alidixic acid.
• Transient visual composition.
Steroids
obscuration.
• isual field defects
Enlargement of
blind spot and later
constriction of visual
field.
130 | Ophthalmology
Concept 6.5: Optic atrophy
Learning objectives
• To learn about types of optic atrophy
• To learn about toxic amblyopia

Time Required
1 reading
st
20 mins
2nd look 5 mins

Optic Atrophy:
t is the end result of any pathological process that damages the axons coursing between
retinal ganglion cells and GB
P ima o tic at o h econ a o tic laucomatous o tic onsecuti e o tic
at o h at o h at o h
halky white in color, isc is dirty white in Pathologically - ale waxy disc.
disc margins are clear colour, with blurred Cavernous optic atrophy
margins

x rauma x papillitis or x Retinitis pigmentosa

oxins papilloedema
Tumours
Nutritional

Fig.6.14: PRIMARY OPTIC ATROPHY Fig.6.15: SECONDARY OPTIC ATROPHY

 rophthalmology | 131

Fig.6.16: GLAUCOMA OPTIC ATROPHY Fig.6.17: CONSECUTIVE OPTIC ATROPHY

o ic m l opia o ic ptic eu opath

efers to conditions in which optic nerve fibres are damaged by exogenous poisons.
ts mostly bilateral and clinically leads to retrobulbar neuritis

Causes:
• Tobacco- Cyanide acts as a toxic agent which causes degeneration of the ganglionic
cells of the macular area
• Ethambutol.
• Deficiency of itamins- Thiamine, B12
• Ethyl alcohol.
• ethyl alcohol- ethyl alcohol poisoning is more dangerous than ethyl alcohol because
it leads to direct damage of ganglion cells.
• Quinine.
• Chloroquine.
• Isoniazid.
• Digoxin.
• NSA Ds.
132 | Ophthalmology
Concept 6.6: Supranuclear Disorder of Eye Movement
Learning objectives
• To learn about features of Supranuclear eye Disorder
• To learn about nternuclear ophthalmoplegia and one and half syndrome

Time Required
1 reading
st
20 mins
2nd look 5 mins

Features are:
• Ga e palsies.
• Normal vestibulo-ocular reflexes.
• Absence of diplopia.
Hori ontal Ga e Centre: t is located in pons, known as PP F i.e. Pontine Parareticular
Formation. PP F controls the lateral rectus of the same side whereas the medial rectus
of the opposite side is controlled by F edial ongitudinal Fasciculus . esion of F
leads to nternuclear Ophthalmoplegia

nte nuclea phthalmople ia

• Due to lesion of F i.e. edial ongitudinal Fasciculus.
• Defective adduction of ipsilateral eye.
• Ataxic nystagmus of the contralateral abducting eye.

Right Medial Longitudinal

BASELINE
fasciculus lesion (MLF)

Right Internuclear
Ophthalmoplegia (INO)

Left abduction
nystagmus magnus

R L

Fig.6.18:
 rophthalmology | 133
One And A Half Syndrome:
t occurs due to lesion of PP F and F of the same side.
An alternative anatomical cause is a lesion of the abducens nucleus on one side
resulting in a failure of abduction of the ipsilateral eye and adduction of the contralateral
eye conjugate ga e palsy towards affected side , with interruption of the ipsilateral
medial longitudinal fasciculus after it has crossed the midline from its site of origin in the
contralateral abducens nucleus resulting in a failure of adduction of the ipsilateral
eye .

Right one BASELINE

and half
syndrome

Left abduction nystagmus

Fig.6.19:
134 | Ophthalmology
Concept 6.7: Nystagmus
Learning objectives
• To learn about basic types of nystagmus

Time Required
1st reading 20 mins
2 look
nd
5 mins

t is the repetitive, involuntary to and fro oscillation of the eyes.

Clinical Types:
a. Pendular:
elocity is equal in each direction.
b. Jerk:
Has slow drift and a fast phase.
c. ixed:
Pendular in primary position and jerk in lateral ga e.

Causes:
a. Physiological:
ƒ Optokinetic nystagmus [OKN]. t consists of saccadic and pursuit movements.
Defect in O N indicates parietal lobe lesion
ƒ End gaze
ƒ Vestibular – COWS (cold water induces nystagmus to opposite side)
b. otor mbalance:
ƒ Congenital nystagmus.
ƒ Spasmus nutans: t is associated with head nodding.
ƒ atent nystagmus: In Infantile Esotropias
ƒ Ataxic nystagmus n nternuclear ophthalmoplegia
ƒ See-saw nystagmus: seen in patients with bitemporal hemianopia.
c. Ocular Nystagmus: Due to sensory deprivation.
 rophthalmology | 135
Worksheet
• DO TH S CHAPTE F O D B

• E T A PO NTS F O D B


136 | Ophthalmology
• Fill in the visual field defects
tic a iations
• Lesions of Temporal Radiations--------
• Lesions of Parietal Radiations-----------
cci ital o te
• Occlusion of posterior cerebral artery-
• Occlusion of middle cerebral artery-

T pat a afferent ner e efferent ner e

• dentify
 rophthalmology | 137
• A miotic pupil remains miotic in dark. ikely pathology
• Sympathetic pathway –
ƒ Central ,
ƒ Pre ganglionic – ,
ƒ Post-ganglionic –
• rite some features of the diagnosis

• ost common cause of optic neuritis is

• hich are these optic neuritis

138 | Ophthalmology
Fill in the blank spaces
P ima o tic at o h econ a o tic laucomatous o tic onsecuti e o tic
at o h at o h at o h

ite some u s causin to ic neu opath

 rophthalmology | 139
Where is the lesion?
BASELINE

Left abduction
nystagmus magnus

R L
140 | Ophthalmology
EXTRA POINTS:
7 Glaucoma

CONCEPTS
 oncept e nitions and asic p siolo

 oncept n esti ations in lauco a

 oncept pen an le lauco as

 oncept losed an le lauco as

 oncept Treat ent odalities in lauco a

 oncept e elop ental lauco as

 oncept econdar lauco as

142 | Ophthalmology
oncept efinitions an asic ph siolo
earnin ob ecti es
• To know about different terms in glaucoma
• To learn basic acqueous physiology

ime e ui e
1st reading 35 mins
2 look
nd
10 mins

efinition
Glaucoma is a multifactorial optic neuropathy in which there is characteristic optic nerve
damage

o mation an aina e of ueous umou

ate of Formation: 2. l/minute. Formation occurs through non-pigmented epithelial
cells by Pars plicata of ciliary body.
• By secretion.
• By ultrafiltration.
• By diffusion.
 la oma | 143
Aqueous humour consists of: Proteins, Na , , g , rea and Glucose ess than
blood plasma . Cl, lactate, pyruvate, Bicarbonate, Ascorbate ore than blood plasma .

lassification

Primary Glaucoma
lauco as
Secondary Glaucoma

Developmental
Glaucoma

Primary Glaucoma
• Open angle Primary open angle Glaucoma IOP high, VF and OD changes+
Normal tension Glaucoma IOP Normal, VF and OD changes+
Ocular Hypertension IOP high, VF and OD Normal

• Closed angle Primary angle closure suspect IOP , VF and OD Normal

Primary angle closure IOP high, VF and OD Normal
Primary angle closure glaucoma IOP high, VF and OD changes+
Secondary glaucoma
Developmental glaucoma Primary congenital Glaucoma

Glaucoma associated with congenital

anomalies/ syndrome

P nt aocula essu e isual fiel o tic isc

closed angle

ar tra
b e cut k b
me ecuta
tra hwor shw r
s ork
me

i
144 | Ophthalmology
oncept n esti ations in laucoma
earnin ob ecti es
• To know about investigations done in glaucoma patient

ime e ui e
1st reading 60 mins
2 look
nd
25 mins

onioscop
Bimicroscopic examination of anterior chamber angle
Indirect ngle is examined by re ected light
Ex- Goldman, Zeiss, Posner, Susman
Direct Keoppe, Barkan, Thorpe and Swan Jacob goniolenses

Identification of Angle Structures on Gonioscopy (From Anterior Posterior):

• Schwalbe’s line
• Trabecular meshwork
• Scleral spur
• Ciliary body
• oot of ris

a in of ante io cham e an le ase on on e ic i e i is to co neal

an le sepa ation
Grade 4 Wide open angle (Iris to cornea angular separation of 35-45 degree)
Grade 3 Moderately open angle (Iris to cornea angular separation of 20-35 degree)
Grade 2 Moderated narrow angle (Iris to cornea angular separation of 20 degree)
Grade 1 Extremely narrow angle( Iris to cornea angular separation of 10 degree).
Grade 0 Closed angle (Iris to cornea angular separation of 0 degree).

mage of ridocorneal Angle

Gonioscope
Gonioscope irror

Ocular
ubricant Cornea
ridocorneal
Angle
ens ris

i i
 la oma | 145
Normal Anterior chamber depth is 2- mm.
Deep anterior chamber: yopics, ales.
Shallow anterior chamber: Hypermetropes, Old people, Females

easu ement of P
• old ann
• er in
• c iot
• al alo
• on contact
• ra er
pplanation ndentation

pplanation
• Tonopen and na ic
• a a ar ndentation ontour
• PASCAL

not er t pe ebound tono eter is o e based

old ann is old standard tono eter
Tono rap t is used to measure the facility of aqueous outflow’

i S

i P S
146 | Ophthalmology

i i tonomete

i P

i Schiot

i P S S
 la oma | 147
aluation o ptic er e ead

isual ield Testin eri etr

inetic
• ister
• Tangent Screen / Bjerrum Screen

Static
• Automated Perimetry
ƒ Octopus
ƒ Humphey field analyser
Combined kinetic and static: Goldmann Perimeter
Campimetry: Central visual field evaluation Central 0

i Confrontation visual i Goldmann kinetic Perimeter i Humphrey automated

fiel exa perimetry static
148 | Ophthalmology
P o ocati e ests
For PACG For POAG
• Mydriatic test: Rise in IOP of >8mmHg after instillation of Water drinking test
tropicamide

• Dark Room/ prone provocative test: Patient in dark room for 60-90
min. If >8 mmHg in IOP; test is +ve

• Phenylephrine: Pilocarpine test: 10% phenylephrine and 2% pilo-

carpine – causes middilated pupil
 la oma | 149
oncept pen an le laucoma
earnin ob ecti es
• To learn about different entities in open angle glaucoma
• To learn signs and management in open angle glaucomas

ime e ui e
1 reading
st
50 mins
2nd look 20 mins

pen n le laucoma
is facto s
• Heredity.
• Age - common elderly.
• yopes
• Diabetics
• Hypertension
• Cigarette smoking.
• Thyrotoxicosis.
ise in OP is due to decreased outflow of aqueous humour from the trabecular meshwork
– This is due to thickening and sclerosis of trabeculae and absence of giant vacuoles in
the cells lining schlemn canal.

linical eatu es
• ild headache/Eye ache
• Di culty in reading and close work
• Frequent change of presbyopic glasses
• Delayed dark adaptation

Si ns
P han es
ncrease in OP The normal range of OP is between 10- 21mmHg
Exaggeration of normal diurnal variation of OP of mmHg Normal variation is around
5mmHg

ptic isc han es in laucoma

• Assymmetry of cup.
• Flam shaped haemorrhages at disc – splinter hemorrages in NTG
• etinal nerve fibre layer damage/atrophy
• ncrease Cup: disc ratio of 0. to 0.
• Thinning/Notching of neuroretinal rim
• Bayonetting sign : double bending of vessels
• Pulsation of retinal arterioles at disc margins
• amellar dot sign ie pores in lamina cribrosa
150 | Ophthalmology
P S

i Normal optic nerve head i laucomatous cuppin

i NASAL BENDING OF BLOOD VESSELS i S

AND BAYONETTING SIGN
isual iel efects

i SP i o mal etinal fi es
 la oma | 151

i VISUAL FIELD DEFECTS in Glaucoma

• sopter contraction: Earliest but non specific visual field defect. ild constriction of
central and peripheral field.
• aracentral scoto a: Small ring shaped sotoma which happens to be either above
or below the blind spot in bjerrum’s area. Earliest clinically significant field defect.
152 | Ophthalmology
• iedel s scoto a: t is a sickle shaped scotoma formed by paracentral joining of
the blind spot.
• erru s or rcuate scoto a: Extension of scotoma in the area either above or
below the fixation point.
• ouble arcuate or rin scoto a: hen two arcuate scotomas join together, it is
called double arcuate scotoma.
• oenne s central nasal step: Two arcuate scotomas run in different arcs and meet
to form a sharp right angled defect

Te poral isual eld is last to be affected in lauco a

or al Tension lauco a or al isc an es ield de ects

cular pertension o disc c an e o eld de ects

Treat ent o and T edical management aser trabeculoplasty

Surgery
 la oma | 153
oncept lose an le laucoma
earnin ob ecti es
• To learn about different entities in closed angle glaucoma
• To learn signs and management in closed angle glaucomas

ime e ui e
1 reading
st
30 mins
2nd look 10 mins

n le losu e laucoma
• Sex - Females are more prone. Female: ale- :1.
• Family history - Positive.

P e isposin anatomical is acto s

• Hypermetropic eyes with shallow anterior chamber.
• ris - ens diaphragm placed anteriorly.
• Plateau iris configuration
• arge lens
• Small corneal diameter.

P S an P
The patient is asymptomatic but sometimes can complain of halos around the lights and
transient ha iness of the vision. This happens when some part of the angle closes when
the pupil is mid dilated and then reopens. Only during the closure, the patient complains
of such symptoms. Otherwise the eye is white and quiet.

P
Characteri ed by all the features of open angle glaucoma i.e. OP changes, fundus
changes and field defects, but the angle is closed.
Treat ent o an le closure aser peripheral iridotomy edical management
Surgery
cute con esti e acute an le closure lauco a
Dim light or pupil mid dilating precipitate the pupil block and lead to high rise in OP.

eatu es
• hole 60 degree angle is closed.
• Patient suffers from severe pain associated with nausea and vomiting.
• The OP is in the range of 60 mmHg 0- 0 mm Hg .
• Coloured halos due to corneal edema
• Severely congested eye associated with lid oedema.
• Shallow AC.
• Closed angle
• ertically oval semidilated pupil - non reactive to light
154 | Ophthalmology
• Field defects are not prominent in this stage
• ogt’s Triad:
• Pigment dispersion on the corneal endothelium
• Sector iris atrophy
• Glaucomaflecken

efiniti e t eatment of choice is su e ase pe iphe al i i otom a

angle open to
trabecular meshwork
tra
b
me ecuta
shw r
ork

Before going on for surgical procedures, it is important to control the raised OP.
mannitol or aceta olamide is used for this purpose. Once the OP is down, laser/
surgical procedure is performed
bsolute lauco a: t’s a painful blind eye. The eye is stony hard. Cyclophotocoagulation
is done to decrease OP.
 la oma | 155
oncept eatment mo alities in laucoma
earnin ob ecti es
• To learn about different treatment options in glaucoma
• To know major side effects of glaucoma medications

ime e ui e
1 reading
st
60 mins
2nd look 25 mins

e ical the ap
Drugs Mechanism of action i e e ects
beta blockers Decrease aqueous production Precipitation of bronchial asthma
Selective: Betaxolol. Arrhythmias
Non- selective: Timolol Dry eyes
Nasolacrimal duct blockage
Miotics: Pilocarpine ncrease trabecular out ow Uveitis
Ciliary spasm
Myopia
Cataract
Iris cyst
Retinal detachment
Sympathomimetics: Decrease aqueous Allergic conjunctivitis
Non selective- Adrenaline, production Angle closure glaucoma
dipivefrine ncrease uveoscleral out ow Adrenachrome deposition
Selective –Brimonidine, Aphakic cystoid macular edema
Apraclonidine Drowsiness
Lid retraction
Carbonic anhydrase inhibitors Decrease aqueous C/I in sulfa drug allergics.
Dorzolamide and Brinzolamide production Acetazolamide: Hypokalemia,
(Topical). Acetazolamide metabolic acidosis, kidney stones,
(Systemic). chronic renal failure.
Dorzolamide and Brinzolamide:
corneal decompensation.
PG analogues: Increase uveoscleral Uveitis
Latanoprost, Travoprost, out ow Iris hyperchromia
Bimatoprost Blephroconjunctivitis
Trichomegaly
Hyperosmotics: Dehydrates vitreous Decompensation in congestive heart
Mannitol, glycerol failure, pulmonary edema
156 | Ophthalmology

i HYPERPIGMENTED IRIS BY PROSTAGLANDIN ANALOGUES

i HYPERTRICHOSIS BY i Lid retraction by alpha agonists

PROSTAGLANDIN ANALOGUES

i BLACK CONJUCTIVAL DEPOSIT BY EPINEPHRINE

e e laucoma ents
hopressa netarsudil 0.02 ophthalmic solution – it inhibits rho-associated protein
kinase OC increases drainage and norepinephrine transporter NET reduced
aqueous production
y ulta latanoprostene bunod 0.02 ophthalmic solution - increasing aqueous humor
outflow through both the trabecular meshwork via nitric oxide, and the uveoscleral route
via latanoprost
 la oma | 157
ase he ap
r on aser Trabeculoplast aser burn to trabeculum at the junction of the
pigmented and non-pigmented parts – increases drainage of acqueous, more useful in
open angles with pigmented trabecular meshwork like pigmentary or pseudoexfoliation
glaucoma

ase i i otom

i LASER IRIDOTOMY

Su ical eatment
Trabeculecto Creation of new channel for aqueous outflow between the anterior
chamber and subtenon’s space

Bleb Diagram showing

flow of aqueous
through a normal
Ostium trabeculectomy

Flow of aqueous

i TRABECULECTOMY

nti etabolites in Trabeculecto t is used in cases in which there is high risk of

failure of the surgical procedure.
a. 5- F .
b. itomycin C.

tificial filte in Shunts Setons

t is used in cases where conventional filtering procedure has failed or likely to fail.
These are plastic devices which create a communication between the anterior chamber
and sub- tenon’s space.
158 | Ophthalmology
• Express
• olteno mplant.
• Schoket mplant.
• Ahmed Glaucoma alve AG
• en
• iStent

P S

i AHMED VALVE i AHMED VALVE

i ISTENT

i XEN implant (SUBCONJUNCTIVAL bypass)

 la oma | 159
oncept e elopmental laucoma
earnin ob ecti es
• To learn about features of congenital glaucoma

ime e ui e
1st reading 20 mins
2 look
nd
10 mins

ri ar on enital lauco a: nheritance is- A Autosomal ecessive

True Congenital.
Infantile Before 3 years of age.
Juvenile 3 - adolesence.

e elopmental anomal of an le of ante io cham e a eculo s enesis

Clinical features
Photophobia, blepharospasm, lacrimation
Buphthalmous
Corneal enlargement - (>13 mm) Haab’s Striae - break in DM, Corneal edema
Blue and thin sclera
Deep AC
Flat lens; which may sub-luxate.
IOP - Raised but neither marked nor acute.
Enlarged C:D ratio may be either due to neuronal loss or enlargement of scleral canal - reversible

i
160 | Ophthalmology
eatment
• Goniotomy - t is the choice of surgery done for congenital glaucoma. n this procedure
cuts are given through the angle.
• Trabeculotomy - t is the procedure to cut open the schlemn canal. t is done if
corneal ha e is there and angle not visualised
• Combined trabeculotomy and trabeculectomy

Secon a on enital laucomas

• ith irido-corneal dysgenesis: Axenfeld’s anomaly, iegers anomaly, Peter’s anomaly
• ith Aniridia.
• Associated with ectopia-lentis syndromes
• Nanophthalmos.
• Naevus of ota
• owe’s syndrome.
• Phacomatosis: Sturge - eber syndrome, on- ecklinghausen’s Disease.
 la oma | 161
oncept Secon a laucomas
earnin ob ecti es
• To learn about features of congenital glaucoma

ime e ui e
1st reading 30 mins
2 look
nd
15 mins

ens n uce laucoma

Phacomorphic Glaucoma Intumescent lens –swollen lens block meshwork
Phacotopic glaucoma Subluxation or dislocation of lens.
Phacolytic Glaucoma orgagnian cataractous lens eakage of lens protein through
intact capsule logging of trabecular meshwork by lens
proteins and macrophages.
Lens Particle Glaucoma/Phacotoxic Rupture of lens capsule ens particle in aqueous humour
Glaucoma Clogging of trabecular meshwork.

n ammato laucoma
ue to eitis
Secondary ACG with pupil Secondary ACG without pupil Secondary OAG
block block
Due to posterior synechiae. Due to anterior synechiae. n ammatory cells blocking
meshwork

Pi menta laucoma
• n pigment dispersion syndrome.
• Pigments block the trabecular meshwork, iris transillumination, rukenburg spindles
• Treatment- On lines of POAG.

Pseu o foliati e laucoma laucoma apsula e

• Due to deposition of grey dandruff- like material in the trabecular meshwork.
• Treatment - On lines of POAG.

eo ascula laucoma
Associated with neovascularisation of iris ubeosis iridis .

auses
• D .
• C O.
• Eales disease.
• Sickle - Cell retinopathy.
162 | Ophthalmology
Treat ent Panretinal photocoagulation with Artifical shunt operation.

Ste oi n uce laucoma

t occurs due to accumulation of mucopolysaccharides in the trabecular meshwork.

aumatic laucoma
lunt in u
• Angle ecession Glaucoma
• nflammatory Glaucoma
• Due to intra-ocular haemorrhage:
Red cell Glaucoma Due to RBCs.
Haemolytic Glaucoma Due to macrophages laden with RBCs
Ghost cell Glaucoma In vitreous haemorrhage.
Hemosiderotic Glaucoma Due to iron from phagocytosed haemoglobin

ilia loc laucoma ali nant laucoma

ncreased OP with shallow or absent anterior chamber. t occurs due to sequestration of
aqueous humour into the vitreous cavity. t can be seen after trabeculectomy or cataract
surgery

laucoma associate ith i i oco neal en othelial s n omes t s a

p olife ati e en otheliopath
he isease has th ee fo ms
Progressive Iris Atrophy There is stromal atrophy and hole formation in the iris.
Cogan-Rhese syndrome t is characteri ed by diffuse naevus and pedunculated
nodules in the iris.
Chandler’s syndrome Corneal changes are more prominent leading to corneal
edema.

i HYPHEMA i PSEUDOEXFOLIATION GLAUCOMA

 la oma | 163

i PIGMENTARY GLAUCOMA (IRIS ILLUMINATION)

Cornea
Ciliary Body

Aqueous
ens

itreous

Aqueous

i AQUEOUS MISDIRECTION SYNDROME/ MALIGNANT GLAUCOMA

i NEOVASCULARISATION INDUCED
164 | Ophthalmology
o sheet
• DO TH S CHAPTE F O D B

• E T A PO NTS F O D B


 la oma | 165

Primary Glaucoma
• Open angle ____________________ IOP high, VF and OD changes+
Normal tension Glaucoma _____________________
Ocular Hypertension IOP high, VF and OD Normal

• Closed angle ____________________ IOP , VF and OD Normal

_____________________ IOP high, VF and OD Normal
Primary angle closure glaucoma IOP high, VF and OD changes+

ill in the onomete s an p inciples

pplanation ndentation

pplanation
and
ndentation
• PASCAL

• tono eter is o e based

• hich laser is used to do this

166 | Ophthalmology
• hich drug can cause this

• Earliest clinically significant field defect in glaucoma

• This sign is seen in which glaucoma

• hich implant is this

 la oma | 167
• denti t e striae

ite some featu es of con enital laucoma

at is t is si n

ill in
Red cell Glaucoma
Haemolytic Glaucoma
Ghost cell Glaucoma
Hemosiderotic Glaucoma
168 | Ophthalmology
P S
 8 Orbit

CONCEPTS
 Concept 8.1 Orbit Anatomy

 Concept 8.2 Orbital Fissures

 Concept 8.3 Blow out Fracture of Orbit

 Concept 8.4 Proptosis

 Concept 8.5 Dysthyroid Ophthalmopathy

 Concept 8.6 Developmental Glaucomas

 Concept 8.7 Orbital Cellulitis

 Concept 8.8 Retinoblastoma

170 | Ophthalmology
Concept 8.1: Orbit anatomy
Learning objectives
• To know about different bones making orbital walls

Time Required
1st reading 20 mins
2 look
nd
5 mins

Bony orbits are quadrangular, truncated pyramids with volume of 0cc

Fig.8.1:
a Simplifed geometry of the orbits b The orbits from above

edial
wall

ateral
ateral wall wall

edial
wall
Floor

Fig.8.2:

Orbital walls and bones

Medial wall Thinnest medial wall is formed by:
• frontal process of maxilla,
• lacrimal bone,
• orbital cribiform plate of ethmoid body of sphenoid
Floor • Orbital surface of maxillary bone
• orbital surface of zygomatic bone
• palatine bone
It is commonly involved in blow-out fracture
Lateral wall • Zygomatic bone
• greater wing of sphenoid
Superior wall (roof) • Orbital plate of frontal bone
• lesser wing of sphenoid
 Orb t | 171
oncept ital fissu es
Learning objectives
• To know about different fissures in orbit and relates syndromes

Time Required
1st reading 30 mins
2 look
nd
10 mins

n erior orbital ssure Between floor and lateral wall

uperior orbital ssure t is at orbital apex, lateral to optic foramen. Between 2
wings of sphenoid
Optic canal/Optic fora en Formed by lesser wing of sphenoid at orbital apex

Fig.8.3: Structures passing through superior orbital fissure and inferior orbital fissure
172 | Ophthalmology
Supe io o ital fissu e S n ome
t is also known as ochen-Duvigneaud syndrome: is a collection of symptoms caused
by compression of structures just anterior to the orbital apex. Cranial nerves passing
through superior fissure: rd, th, -1, th.

Clinical features:
• Onset is slow
• Proptosis ptosis masked by proptosis
• Dereased corneal sensation due to -1/ ophthalmic branch of trigeminal nerve .
• Ophthalmoplegia due to , and nerves
rbital pe ndro e Orbital apex superior orbital fissure syndrome involvement
of optic nerve
 Orb t | 173
Concept 8.3: Blow out fracture of orbit
Learning objectives
• To know different ray views and blow out fracture

Time Required
1st reading 20 mins
2 look
nd
5 mins

Blow-Out Fracture:
t is the fracture of orbital floor which typically occurs by a sudden increase in the orbital
pressure by a striking object 5 cm in diameter such as a fist or tennis ball.

Two types:
• Pure blow-out fracture -Does not involve the orbital rim.
• mpure blow-out fracture - nvolves the rim

Fig.8.4: Tear drop sign

Clinical Features:
• Ecchymosis
• Subcutaneous emphysema: t occurs only if medial wall is also fractured.
• Enophthalmos.
• nfraorbital nerve anesthesia: t leads to decreased sensation on the affected cheek.
• Diplopia.
• Tear drop sign

Treatment:
• Conservatively by antibiotics and anti-inflammatory.
• Surgery: f no improvement in enophthalmos or diplopia then surgical intervention
is needed.
174 | Ophthalmology
X-Ray Views of Orbit:
NAME VIEWS STRUCTURES SEEN
Caldwell-luc view PA View Superior orbital fissure.
Occipitofrontal reater and lesser wing of sphenoid. thmoid
and frontal sinus.
loor of sella.
Town’s view view. rontooccipital orsum sellae of sphenoid bone.
nferior orbital fissure.
Water’s View ccipito meatal. axillary sinus and oor of orbit. in blow out
fractures)
Rhese view or optic foramen.
 Orb t | 175
Concept 8.4: Proptosis
Learning objectives
• To know about different tests and examples of proptosis

Time Required
1st reading 40 mins
2 look
nd
15 mins

Proptosis
Forward protrusion of normal- si ed eyeball 21 mm beyond the lateral orbital margin
or 2mm protrusion compared to the other eye.

Measurement of proptosis:
Nafzigger test Inspection of the eyeballs from behind the patient looking over his
forehead.
Hertel’s Exophthalmometre To measure the distance between the apex of cornea and lateral orbital
margin.
Leude’s Exophthalmometre t is useful in children.
Topometre seful for non axial proptosis.
Simple plastic rule

Fig.8.5: Hertel’s EXOPHTHALMOMETRY Fig.8.6: Naf igger test

Bilateral proptosis
Painful Cavernous sinus- thrombosis
Painless Grave’s disease
Pseudotumor
Lymphoma
arotico cavernous fistula
Leukemia
Metastasis
Developmental anomalies
176 | Ophthalmology
Unilateral proptosis
Painful Painless
Axial • rbital haemorrhage. • Hemangioma
(central • rbital cellulitis. • Meningioma
protusion) • Orbital mucocoele • Glioma
• Cavernous sinus thrombosis • Schwanoma
• Pseudotumor
Non-axial • Adenoid cystic carcinoma of lacrimal • Down and medial- Dermoid, lacrimal
(non-central gland gland tumors
protusion) • Nasopharyngeal carcinoma • Down and temporal - Frontoethmoid
• Metastasis mucocoele, lacrimal sac tumours
• Superior - Maxillary sinus tumor and
mucocele.

Pseudoproptosis:
The eye ball appears to be proptosed by actually there is no forward displacement.
• High axial myopia
• Shallow orbit due to craniofacial synostosis
• etraction of the upper eyelids
• Enophthalmos of the other eye
 Orb t | 177
Concept 8.5: Dysthyroid Ophthalmopathy
Learning objectives
• To know about signs of Thyroid eye disease

Time Required
1st reading 40 mins
2 look
nd
15 mins

ay or may not be associated with hyperthyroidism. The patient may be euthyroid,

hyperthyroid or hypothyroid

Fig.8.7: Axial proptosis Fig.8.8: Superior limbic keratoconjunctivitis

Fig.8.9: on raefe s Sign (Right E e)

Normal Grave's ophthalmopaty

Retroorbital
fat

Retroorbital
muscles

Fig.8.10
178 | Ophthalmology

Eye Lid Signs Soft tissue Proptosis Restrictive thyroid optic

involvement myopathy neuropathy

The earliest and • Conjunctival It can be axial or nlargement of Due to

most common in ection. non- axial/ xtraocular muscle compression
symptom is upper • hemosis. painful or painless/ without enlargement of optic nerve
eyelid retraction • dema and unilateral or of tendon is the at orbital apex
alrymple s sign fullness of bilateral hallmark by increased
Fibrosis of the eyelids. It is due to the intraorbital
inferior rectus deposition of pressure
• Superior limbic Kocher’s sign-
leads to rebound keratoconjunc- mucopolysachharides
Staring appearance
overaction of SR- tivitis of eyes. Sequence of
LPS complex involvement of
Stellwag’s muscle is R R
sign- Decreased SR R.
frequency of
blinking. Patient presents with
diplopia and squint.
Treatment: Treatment: Treatment: Restrictive myopathy RAPD+
Surgical. • Tear substitutes If progressive and is diagnosed by Treatment
Medical: • For superior painful: orced uction est. -Intravenous
Topical limbic kerato- Systemic Steroids. steroids
guanethidine conjunctivitis Radiotherapy:
- depletes • Acetylcysteine For its anti-
sympathetic storage [It dissolves the in ammatory
sites. mucus . effect.
Chemodeneravation Surgery:
of LPS by Decompression
botulinum toxin surgery
 Orb t | 179
Concept 8.6: Orbital tumours
Learning objectives
• To know features of few important intraorbital tumours

Time Required
1st reading 40 mins
2 look
nd
15 mins

Lacrimal Gland Tumors:

Benign:
ost common tumor of lacrimal gland is Pleomorphic adenoma mixed -cell tumor . acrimal
gland tumor cause non-axial proptosis i.e. down and medial dis- placement of eyeball.

Malignant:
• Adenoid cystic carcinoma : t is the most common malignant tumour, painful as there
is perineural invasion.
• Pleomorphic adenocarcinoma
• ucoepidermoid carcinom

Fig.8.11: LACRIMAL GLAND TUMOUR

Optic nerve tumours

Optic Nerve Glioma Optic nerve sheath meningioma
Common in children, Female > males 3rd-5th decade of life, Female > males
Majority are of astrocytic origin Arises from meningothelial cells
25-50% patients have associated neurofibromatosis
neurofibromatosis
Nearly 75% of optic nerve gliomas arise from optic
chiasma and adjacent optic nerve while 25% arise
from orbital part of optic nerve.
resentation is generally with visual loss, R . nilateral loss of vision gradual in onset .
Slow growing tumor; proptosis is a late feature Optociliary shunt
Optic atrophy
Imaging - Fusiform enlargement of nerve along with Imaging - Tubular appearance of nerve along with
enlargement of optic canal. calcification
180 | Ophthalmology
For both-Treatment:
1. Observation.
2. Surgery.
. adiotherapy.

Fig.8.12: OPTIC NERVE GLIOMA Fig.8.13: OPTIC NERVE SHEATH

MENINGIOMA

Most common benign intraorbital tumor in children is – Dermoid

ost common primary malignant orbital tumor in children is Rhabdomyosarcoma.
ost common cause of benign intraorbital tumour in adults avernous hemangioma.
Most common primary malignant orbital tumor in adult is – Lymphoma

Fig.8.14: DERMOID CYST Fig.8.15: CAPILLARY HEMANGIOMA

Fig.8.16: RHABDOMYOSARCOMA Fig.8.17: CAVERNOUS HEMANGIOMA

 Orb t | 181
Concept 8.7: Orbital cellulitis
Learning objectives
• To know features and classification of orbital cellulitis

Time Required
1st reading 30 mins
2 look
nd
10 mins

Orbital Cellulitis
t is the inflammation in the orbit behind the orbital septum.

Fig.8.18:

Etiology Clinical features Treatment

• Sinusitis- Most commonly • U/L painful proptosis- Abrupt • Admit the patient as it is an
after ethmoid sinusitis. onset. ocular emergency.
• From adjacent areas like • Restriction of extraocular • Parenteral antibiotics , both
Dacryocystitis movements aerobic and anaerobic with full
• Mid-facial infections and • iplopia. coverage for gram positive and
dental infections. gram negative organisms.
• Post-traumatic- Any injury that
penetrates the orbital septum.
It occurs after 48-72hrs after
injury
• Post-surgical
182 | Ophthalmology
han le classification fo o ital cellulitis
1 n ammatory yelid edema and erythema
edema NormaJ extraocular movement
Normal visual acuity
II Orbital cellulitis iffuse edema of orbital contents without discrete abscess
formation
III Subperiosteal Collection of purulent exudate3 beneath periosteum of lamina
abscess papyracea
Displacement of globe downward/laterally
IV Orbital abscess Purulent collection within orbit3
Proptosis
Chemosis
Ophthalmoplegia
Decreased vision
V Cavernous sinus ilateral eye findings
thrombosis Prostration
Meningismus

Cavernous Sinus Thrombosis

Clinical features:
• astoid tenderness
• Cerebral symptoms with vomiting and rigor – meningismus
• nvolvement of opposite eye –first being paralysis of sixth nerve, hence limited
abduction of the other eye.
• Decreased corneal and cheek sensation due to the involvement of the fifth nerve.
• Complete limitation of eye ball movement due to involvement of rd, th and 6th
nerves.
• Pupil dilated and fixed due to involvement of the third nerve.
• Disc edema
• Engorgement of retinal veins.
• apidly developing proptosis.
 Orb t | 183

Ant. cerebral a.
nt. carotid a.

Ant. clinoid process

Subarachnoid
space

Optic
chiasma
Oculomotor n.
Trochlear n.
Hypophysis
Oculomotor 1
n.

axillary 2
n.
Sphenold
sinus Pia

Arachnold

Dura

Abducens n.

Fig.8.19: CAVERNOUS SINUS

T T agnetic resonance angiograohy is the investigation of choice which

will show absence of flow in thrombosed sinuses.
Treat ent / Antibiotics. Prognosis is poor.
184 | Ophthalmology
Concept 8.8: Retinoblastoma
Learning objectives
• To learn in detail about retinoblastoma
• To learn orbital surgeries

Time Required
1 reading
st
45 mins
2nd look 15 mins

ost common cause of malignant intraocular tumour in children is – etinoblastoma.

ost common cause of malignant intraocular tumour in adults – Choroidal malignant
melanoma.
etinoblastoma arises from primitive multi-potential neuroectodermal cells of retina.
ost common age of diagnosis is 1 months.

Genetics:
• nheritance – AD, but only 6 cases are familial.
• nilateral in 0- 5 while bilateral is 25 - 0
• Familial cases have early onset, bilateral involvement and are predisposed to develop
non- ocular malignancy including pinealoblastoma and osteogenic sarcoma.
• B/ retinoblastoma with pinealoblastoma is termed as trilateral retinoblastoma.
• The specific area corresponding to retinoblastoma gene was identified on
• 1 band, on long arm of chromosome 1 – i.e. 1 q 1 .
• 1 q syndrome - etinoblastoma when associated with other dysmorphic features
microcephaly, broad nasal bridge, hyperteleorism and mental handicap .
• nudson’s two hit hypothesis: n hereditary retinoblastoma, first genetic change/hit
in B gene is in- herited from an affected parent while second mutation second hit
occurs in post natal life and both alleles are lost.
• n non-hereditary retinoblastoma, both mutations first and second hits occur in post
natal life.

Clinical features:
ode of presentations are:
• eukocoria 60 : t is the most common mode of presentation.
• Strabismus 20 : t is the second most common mode of presentation.
• Secondary glaucoma.
• Pseudouveitis.
• Orbital inflammation - mimicking orbital cellulitis.
• Proptosis.
• Heterochromia iridis, rubeosis iridis.

Growth patterns
• Exophytic: towards choroid
• Endophytic: towards vitreos
• Diffuse infitrating
 Orb t | 185
Pathology:
Gross:
• Chalky white friable mass with dense foci of calcification and necrosis.
• Seeding into vitreous cavity.
• Extension to uvea, epibulbar structures, optic nerve and orbit.

Microscopic:
Basophillic mass with light eosinophillic areas due to necrosis.
A. ell - differentiated:
Flexner- intersteiner rosette specific for retinoblastoma .
Homer- right roset.
Fleurette formation.
Poorly differentiated: Poor prognosis.

Investigations:
-ray- heese view will show enlargement of optic foramen
SG: B scan. t helps to visuali e calcification in tumour.
CT-Scan - for intracranial extension .
- nvestigation to choice to assess spread of tumour via optic nerve .

Enzymes found to be raised in acquous are:

• DH- actic acid dehydrogenase.
• PG - Phosphoglucoisomerase.
• NSE- Neuron- Specific- Enolase

Staging and treatment of retinoblastoma

1 Intraocular Group Findings A-Laser photocoagulation/
Cryotherapy
A Tumor thickness <3 mm
B Tumor thickness >3 mm; located within the temporal
arcade B, C, D- Neoadjuvant
chemotherapy to decrease
C Localized vitreous body or subretinal metastasis
the size of the tumour
D iffuse vitreous body or subretinal metastasis Drugs used are Vincristine,
Massive tumor with no chance of preserving the eye topside and arboplatin
Followed by laser/cryo

enucleation
2 Optic nerve Most common mode of spread is via optic nerve nucleation with
invasion radiotherapy/Chemotherapy
3 Orbital xenteration
extension
4 Distant- Palliative
Metastasis
186 | Ophthalmology
nucleation emoval of the eyeball with long piece of optic nerve
aser otocoa ulation for posterior tumours
r ot erap Tripple free ing - thaw technique, for anterior tumours
ifferential ia nosis o eu ocoria t is collectively known as Pseudogliomas These
are the conditions which simulate retinoblastoma due to the presence of leukocoria
Differentiating features of pseudoglioma from retinoblastoma:
• OP is raise in etinoblastoma while decreased/normal in pseudoglioma
• There is intraocular calcification in retinoblastoma which is not seen in pseudoglioma.
• Congenital cataract.
• PHP Persistent hyperplastic prima- ry vitreous .
• OP etinopathy of prematurity .
• Toxocariasis.
• Coats disease.
• Coloboma of optic nerve.
• etinal astrocytoma: t is the benign counterpart of retinoblastoma.
• Fungal endophthalmitis.
• etinal dysplasias.
Enucleation: Evisceration: Exenteration:
Removal of eyeball with stump Removal of entire intraocular Complete removal of eyeball, the
of optic nerve leaving behind the contents of the eye, leaving the retrobulbar orbital soft tissues,
extra ocular muscles scleral shell and extraocular and most or all of the eyelids, uptil
muscle attachements intact. periosteum
lind painful eye. xpulsive choroidal hemorrage rbital extension of alignancies.
ntraocular tumor. Pan-ophthalmitis ucormycosis.
thisis bulbi. Bleeding anterior staphyloma hronic orbital pain.
icrophthalmia. Severe trauma with risk of rbital deformities.
sympathetic ophthalmitis.

Fig.8.20: Leukocoria Fig.8.21: alcification in etino lastoma

 Orb t | 187
Worksheet
• DO TH S CHAPTE F O D B

• E T A PO NTS F O D B


188 | Ophthalmology
n erior orbital ssure: Between
uperior orbital ssure: Between
Optic canal/Optic foramen: Formed by

• a e so e ner es passin ro upper part o superior orbital ssure and

in erior orbital ssure
• dentify the sign

• Fill in the blank spaces

NAME VIEWS STRUCTURES SEEN
Caldwell-luc view PA View

Occipitofrontal

Town’s view view. rontooccipital

ccipito meatal. axillary sinus and oor of orbit. in blow

out fractures)

Rhese view

• hich test is being done

 Orb t | 189

Name some examples of Bilateral proptosis

Painful
Painless

• hich sign is this in thyroid eye disease

• Earliest muscle involved in thyroid eye disease

• hich sign is this in thyroid eye disease?

190 | Ophthalmology
• hich syndrome its associated with

• rite some features of cavernous sinus thrombosis

ode of presentations of retinoblastoma:

• : t is the most common mode of presentation.
• : t is the second most common mode of presentation

What is this sign?

Fill in
Most common benign intraorbital tumor in children is –
Most common primary malignant orbital tumor in children is –
Most common cause of benign intraorbital tumour in adults-
Most common primary malignant orbital tumor in adult is –
 Orb t | 191
EXTRA POINTS:
 9 lacrimal
EyElids
drainagE systEm
and

CONCEPTS
 Concept 9.1 Eyelid anatomy and muscles

 Concept 9.2 Ptosis

 Concept 9.3 Entropion and Ectropion

 Concept 9.4 Miscellaneous eyelid and eylash

disorders

 Concept 9.5 Lacrimal drainage system

 Ey l d and a r mal dra nag y t m
Concept 9.1: Eyelid anatomy and muscles
Learning objectives
• To know about layers of eyelid
• To learn important muscles in eyelid

Time Required
1 reading
st
20 mins
2nd look 5 mins

Fig.9.1:

Eyelid Anatomy
The eyelid is divided into the upper lid and lower lid. It has 7 layers
ƒ Skin- Thinnest skin in body
ƒ Subcutaneous tissue
ƒ Striated muscles
Orbicularis oculi: Three portions: Orbit, Palpebral (Preseptal and Pretarsal) and
Lacrimal – supplied by 7th nerve
Levator palpebral superioris – supplied by 3rd nerve
ƒ Submuscular areolar tissue- contains veseels and nerves
ƒ Orbital septum and Tarsal plate (Fibrous skeleton of lids containing Meibomian
glands)
ƒ Smooth muscle – Muller
ƒ Palpebral conjunctiva

Fig.9.2: Levator palpebral superioris – elevation of Fig.9.3: Origin: Lesser wing of sphenoid
upper eyelid
 Ophthalmology
Insertion:
• Skin crease
• Medial and lateral palpebral ligaments (including Whitnall’s ligament)
• Anterior surface of tarsal plate

Fig.9.4: ORBICULARIS OCULI –closing of eyelids

 Ey l d and a r mal dra nag y t m
Concept 9.2: Ptosis
Learning objectives
• To know about different types of ptosis
• To learn about management of congenital ptosis

Time Required
1 reading
st
50 mins
2nd look 20 mins

It is drooping of upper eyelid in relation to the globe

Congenital ptosis Acquired Ptosis
Simple congenital ptosis- Neurogenic
• Due to developmental dystrophy of levator muscle. • Third nerve palsy
• Lid lag sign+ • Horner’s syndrome
• Absence of eyelid crease
• Head tilt with chin elevation
Complicated ptosis Mechanical
Marcus gunn jaw-winking syndrome: Increased weight due to tumor, oedema,
• It is due to aberrant connection between the LPS and dermatochalasis
the lateral Pterygoid muscle. It is because of trigemino-
occulomotor synkinesis
Blepharophimosis Syndrome (BPES) Myogenic
• AD • Myasthenia gravis
• Telecanthus (Increased distance between the two medial • Myotonic dystrophy
canthus, but the IPD is normal)
• Ptosis
• Epicanthus inversus (Extra fold of skin on the medial
canthus arising from the lower lid)
• Lower lid ectropion
• Flat nasal bridge with hypoplasia of superior orbital rim
Aponeurotic
Localized dehiscence of aponeurosis
disinsertion-
• Involutional or senile ptosis
• Post operative ptosis
 Ophthalmology

Fig.9.5: CONGENITAL PTOSIS Fig.9.6: Epicanthus

Fig.9.7: Marcus Gunn Jaw Winking Phenomeon Fig.9.8: Blepherophimosis–Ptosis–Epicanthus

inversus

Fig.9.9: NEUROLOGICAL PTOSIS Fig.9.10: MYOGENIC PTOSIS

Fig.9.11: MYASTHENIA GRAVIS

Fig.9.12: MECHANICAL PTOSIS Fig.9.13: INVOLUTIONAL/APONEUROTIC

 Ey l d and a r mal dra nag y t m
Clinical Evaluation:
• ar inal re e distance between upper lid margin and light reflex in primary
gaze
• Amount of ptosis: Mild: 2 mm / Moderate: 3-4 mm / Severe: >4 mm

Fig.9.14:

• PS muscle action pper lid excursion : N 15 mm or more. If it is 4mm or less, it

is poor action

Fig.9.15:
 Ophthalmology
• Bell’s Phenomenon: If Bell’s phenomenon is absent, then it is a contraindication for
surgery
• Tensilon Test: It is done for myasthenia gravis
• Phenylepherine Test: On instilling 10% phenylephrine, if within 10-15 minutes the
ptosis improves, it is due to muller muscle underaction as in Horner’s syndrome
• Upper lid crease: M- 10 mm; F - 8 mm.
• ertical fissure height: : -10 mm, F: -12 mm
Treatment of acquired ptosis – treatment of underlying cause
For mild ptosis-Fasanella: Servat procedure

Fig.9.16:

For moderate ptosis - Levator Resection

Fig.9.17:

Blasckovics operation: Conjunctival route.

Everbusch’s operation: Cutaneous route.
 Ey l d and a r mal dra nag y t m
For severe ptosis -Frontalis Brow Suspension or Sling operation
The material of choice is fascia lata

Fig.9.18:
 Ophthalmology
Concept 9.3: Entropion and Ectropion
Learning objectives
• To know about different causes and treatment of entropion and ectropion

Time Required
1st reading 40 mins
2 look
nd
15 mins

Entropion- It is the inward turning of the lid margin

Involutional Age related No excess horizontal laxity-Weis procedure
(transverse lid split and everting sutures)
Excess horizontal laxity-Quickert’s
procedure (Weis procedure plus horizontal
lid shortening)
Jones procedure
(plication of lower lid retractors)
odified wheelers operation
Cicatrical Cicatrical pemphigoid, Stevens Treat the cause like trichiasis etc
- Johnson syndrome, Trachoma, Tarsal fracture
chemical burns. Mucus membrane grafts

Congenital lower eyelid retractors not well- Hotz procedure

developed
Spastic entropion Treat the cause of the spasm.
Injection of botulinum toxin

ENTROPION

Fig.9.19: INVOLUTIONAL/SENILE ENTROPION Fig.9.20: CICATRICIAL

 Ey l d and a r mal dra nag y t m

Fig.9.21: SPASTIC Fig.9.22: CONGENITAL

Ectropion: Outward turning of eyelid margin

Involutional Age related No horizontal lid laxity — medial
conjunctivoplasty (excision of a diamond of
tarso-conjunctiva)
Mild horizontal lid laxity — Lazy-T
procedure (medial conjunctivoplasty plus full
thickness lid excision)
Severe horizontal lid laxity —
Bick procedure.
odified kuhnt s ymanowski procedure.
Cicatrical Due to trauma, burns Excision of scar with Z- plasty,
transposition aps or free skin grafts.
Congenital lower eyelid retractors not Skin grafts
well- developed
Paralytic Due to facial nerve palsy emporary rtificial tears,ointment
If very poor bells phenomenon- tarsorrhaphy.
Permanent:
• Medial canthoplasty.
• Prosthetic devices - silicone rings

Mechanical Due to eyelid tumours Treat the cause

 Ophthalmology
ECTROPION

Fig.9.23: INVOLUTIONAL/SENILE Fig.9.24: CICATRICIAL

Fig.9.25: PARALYTIC Fig.9.26: MECHANICAL

Fig.9.27: CONGENITAL
 Ey l d and a r mal dra nag y t m
Concept 9.4: Miscellaneous eyelid and eyelash disorders
Learning objectives
• To learn and identify various terminology in eyelids and eyelash disorders

Time Required
1st reading 30 mins
2 look
nd
15 mins

Chalazion (Meibomian Cyst):

t is a chronic lipogranulomatous inflammation of the meibomian glands. t is caused
by blockage of meibomian gland orifices and stagnation of sebaceous secretions. t
presents as a painless swelling on the lid. It is treated by incision and drainage or by
intralesional injection of triamicilone acetate.

Fig.9.28: CHALAZION

External Hordeolum (Stye):

Stye is a small abscess suppurative inflammation caused by an acute staphylococcal
infection of a lash follicle and its associated gland of Zeis or hair follicles. It presents
as a painful swelling at the lid margin. It is treated with hot fomentation, oral anti-
inflammatory and if needed epilation of the hair follicle.

Fig.9.29: STYE
 Ophthalmology
Internum Hordeolum: It is small abscess caused by an acute staphylococcal infection
of meibomian gland. It presents as a painful swelling in the lid. It is treated with hot
formentation, oral antibiotics and anti-inflammatory. ncision and drainage if required,
can be done.
Trichiasis: Misdirection of the eyelashes. It presents as irritation, pain, lacrimation,
blepharospasm. It can lead to punctuate epithelial erosions, corneal ulcer and pannus.
Distichiasis: t is a congenital anomaly characteri ed by extra row of lashes
Symblepharon: It is the adhesion of lid with the globe. It can occur due to burn,
chemical injuries, ulcers or after surgeries.
Ankyloblepharon: Adhesion of the margins of both the lids and both palpebral
conjunctiva. Causes are same as symblepharon.
Lagophthalmos: Inability to close the eyes.
t can lead to exposure keratopathy. Causes are: Cicatri ation of the lids, Paralysis of
orbicularis oculi and proptosis
Madarosis: Loss of eyelashes or loss of eyebrows, both are termed as madarosis.

Causes:
ƒ Local:
ƒ Blepharitis Trachoma, S. J. syndrome.
ƒ nfilterating tumors.
ƒ Burns.
ƒ Radiotherapy or cryoth of lid tumors.
ƒ Skin:
Psoriasis.
Generalized alopecia.
ƒ Systemic:
yxoedema.
Leprosy.
Syphilis.
SLE.
ƒ Following Removal:
Iatrogenic trichiasis.
Trichotillomania.
Poliosis: Whitening of eye lashes is known as poliosis.

Causes:
ƒ Local:
Chronic blepharitis.
Sympathetic uveitis.
ƒ Systemic:
VKH syndrome.
Waardenberg syndrome.
 Ey l d and a r mal dra nag y t m

Fig.9.30: Poliosis Fig.9.31: Distichiasis

Fig.9.32: Symblepharon Fig.9.33: Ankyloblepharon

Fig.9.34: Madarosis Fig.9.35: Lagophthalmous

Malignant Eyelid Tumors:

a. Basal cell carcinoma: It is the most common tumour of the eyelid. Most common site
is lower lid and then medial canthus. It is a slow growing tumour, locally invasive.
b. Squamous cell carcinoma: t is the second most common tumour of the eyelid. t is a
fast growing tumour which metastasizes to the regional lymph node.
c. Sebaceous cell carcinoma: It arises from the meibomian glands. It may present as
Recurrent chalazion.
d. Malignant melanoma.
e. Kaposis sarcoma.
 Ophthalmology
Concept 9.5: Lacrimal drainage system
Learning objectives
• To learn about lacrimal drainage system
• To learn tests for watering eyes
• To learn about dacryocystitis

Time Required
1 reading
st
40 mins
2 look
nd
20 mins

Fig.9.36:

LACRIMAL APPARATUS OF EYE

Fig.9.37:
 Ey l d and a r mal dra nag y t m
Watering of Eyes
Lacrimation: It is the over-production of the tear.
Epiphora- t is overflowing of the tear due to blockage of the drainage system

Causes of Blockage:
Anatomical:
ƒ Strictures.
ƒ Obstruction.
ƒ Foreign body
ƒ Tumor
Physiological:
ƒ Lacrimal pump failure.

Tests of Lacrimal Drainage System:

ƒ Regurgitation test.
ƒ Syringing
ƒ Jones dye test.
ƒ Dacryocystography
ƒ Dacryoscintillography

Syringing/irrigation with saline

Soft stop
Diagnosis: Complete canaliculi block
Re ex from upper canaliculi common canaliculi block
Re ex from lower canaliculi lower canaliculi block
Hard stop
f no saline enters nose mucoid re ux into puncta iagnosis omplete block
If saline enters nose: Possibilities: Hypersecretion, partial obstruction or lacrimal pump

Fig.9.38: JONES DYE TEST 1 Fig.9.39: JONES DYE TEST 2

 Ophthalmology
Jones primary dye test 1
• Positive (dye in nose): Diagnosis: Hypersecretion (1)
• Negative: Possibilities: Partial obstruction or lacrimal pump failure

Proceed with Jones secondary dye test 2

• Positive dye in nose after flushing : Diagnosis: Partial obstruction N D
• Negative: Diagnosis: lacrimal pump failure

Fig.9.40: DACRYOCYSTOGRAPHY Fig.9.41: Arrow pointing towards block

Dacrocystitis:
t is the inflammation of the lacrimal sac at the medial canthus region. t may be:
Congenital chronic or acquired either acute or chronic .

Congenital dacrocystitis:
ƒ It is due to congenital blockade of the lacrimal duct.
ƒ sually presents as mild grade chronic inflammation.

Characterised by:
ƒ Epiphora
ƒ Regurgitation of mucopurulent discharge on applying pressure over lacrimal sac
region, (positive regurgitation test).
ƒ Swelling over the sac area.

Fig.9.42: DACRYOCYSTITIS
 Ey l d and a r mal dra nag y t m
Treatment:
• Upto 9 months -Massage over the lacrimal sac region with topical antibiotics
• months to years -Probing of Nasolacrimal duct:Bowman’s probe is used for this
purpose.
• After 4 years -Dacrocystorhinostomy

Fig.9.43: BOWMAN’S PROBING

Acquired Dacrocystitis:
It may be acute or chronic.
a. Acute dacrocystitis: t is acute suppurative inflammation having marked swelling,
tenderness, redness over lacrimal region with the presence of epiphora.

Treatment:
Cellulitis stage: Systemic and topical antibiotics are given. Systemic anti inflammatory
and analgesics are added along with hot fomentation to relieve pain and swelling.
Lacrimal abscess stage: In addition to above treatment, when the pus starts
pointing out on the skin,it should be drained with a small incision. Later on, either DCR
(Dacrocystorhinostomy)
ternal lacri al stula: After controlling the acute infection with systemic antibiotics,
fistulectomy along with DC .
Chronic dacrocystitis: It is more common than acute form. It occurs as a result of
obstruction of N D due to various causes like chronic inflammation of nasal mucosa or
by polyp pressure etc. Treated by DCR.

Dacryocystectomy – reoval of lacrimal sac - Indications

• lacrimal sac tumor
• Chronic dacryocystitis following failed dacryocystorhinostomy (DCR)
• Dacryocystitis in setting of granulomatosis with polyangiitis (Wegeners granulomatosis)
that is refractory to conventional management
 Ophthalmology
Worksheet
• DO THIS CHAPTER FROM DQB

• E T A PO NTS F O D B


 Ey l d and a r mal dra nag y t m
Levator palpebral superioris –
Action ______________
Origin: __________
Insertion: ___________

Write some features of

Simple congenital ptosis-
•

Whats the diagnosis?

Name some nerves passing from upper part of superior orbital fissure and inferior orbital
fissure
• Which is being tested? _______________________

• Phenylepherine Test in ptosis is done for ________________

• What is the treatment of this? _____________________
 Ophthalmology

• What is the diagnosis and treatment?

• Name the diagnosis

 Ey l d and a r mal dra nag y t m
• Write some indications for Dacryocystectomy

Which test is this?

Treatment of congenital nasolacrimal duct obstruction:

• Upto 9 months -_________________________
• 9 months to 4 years -____________________
• After 4 years -__________________
Ophthalmology
EXTRA POINTS:
10 Uvea

CONCEPTS
 Concept 10.1 Uveal anatomy

 Concept 10.2 Uveitis

 Concept 10.3 Systemic Associations of Uveitis:

Arthritis

 Concept 10.4 Systemic Associations of Uveitis:

Infections

 Concept 10.5 Other Systemic Associations of

Uveitis
216 | Ophthalmology
Concept 10.1: Uveal anatomy
Learning objectives
• To know about basic anatomy of uveal layer

Time Required
1st reading 25 mins
2 look
nd
10 mins

Iris
Circular disc, 12 mm in diameter with an aperture of 3-4 mm called pupil. Its is thinnest
at its root. The anterior surface is divided into ciliary zone and pupillary zone by a zig-
zag line called Collarette (represents attachment of pupillary membrane).

Microscopic:
nterior limiting layer anterior most condensed part of stroma . as melanocytes and fibroblast
Stroma (contains vessels, nerves, sphincter pupillae, dilator muscle)
Anterior epithelial layer
Posterior pigmented epithelial layer.
• Disinsertion of iris from its root is called iridodialysis. The pupil in iridodialysis becomes
D-shaped.
• Aniridia - The iris may be apparently absent, however, a narrow rim exists at the
ciliary border. Wilms tumour is associated with sporadic cases.
• Polycoria –multiple pupil, corectopia – displaced pupil

Fig.10.1: ANIRIDIA Fig.10.2: POLYCORIA/CORECTOPIA

Fig.10.3: IRIDO-DIALYSIS
 a| 217
Ciliary Body
It’s a forward continuation of choroid at ora-serrata.
It is divided into two parts:
• Pars plicata.
• Pars plana.

Microscopic:
Supraciliary lamina outermost condensed stroma , consists of pigmented collagen fibres Stroma consists
of longitudinal, circular and radial fibres and vascular stroma
Layer of pigmented epithelium
Layer of non-pigmented epithelium
nternal limiting membrane.
Accomodation is mainly done by circular and radial muscles. The resting tone of ciliary
muscles is +1D.

Choroid
Extremely vascular membrane. From retina to sclera, it has
• Thin elastic membrane, membrane of Bruch.
• Capillary plexus of fenestrated vessels, the choriocapillaris.
• the layer of medium-sized vessels, while most externally are the large vessels, the
whole being held together by a stroma consisting of branched pigmented connective
tissue cells.
• t is not firmly adherent to sclera - potential space between the two structures - the
suprachoroidal space.
218 | Ophthalmology
Concept 10.2: Uveitis
Learning objectives
• To know about classification of uveitis
• To learn features of different types of uveitis

Time Required
1 reading
st
50 mins
2nd look 20 mins

Uveitis: nflammation of the uveal tract.

lassification
Anatomical Clinical Pathological
Anterior uveitis Acute uveitis: Granulomatous
Intermediate uveitis Sudden onset and persists less than 6 weeks Nongranulomatous
Posterior uveitis Chronic uveitis:
Panuveitis Insidous onset and persists months or years

Fig.10.4:

Anterior Uveitis:
nflammation of iris iritis and anterior part of ciliary body i.e. pars plicata, iridocyclitis .
Most common form of uveitis accounting for 70% cases (approx).
 a| 219
Causes of Anterior Uveitis:
Autoimmune soriasis, ankylosing Spondylitis, n ammatory bowel disease, Sarcoidosis, ehcet s disease.
Infections erpes oster, erpes simplex, , Syphilis, eprosy, leptospirosis.
Malignancy eukemia, retinoblastoma, malignant melanoma, lymphoma
Others diopathic, trauma, uch s heterochromatic iridocyclitis.
Most common cause of anterior uveitis is IDIOPATHIC.

Clinical features:
• Photophobia, pain, redness, decreased vision, lacrimation.
• Circumcorneal (ciliary) congestion
• Keratic precipitates (KP): Proteinaceous cellular deposits at the back of the cornea.
It is a pathognomic sign.
Mutton fat KPs Large and are composed of epitheloid cells and macrophages. Seen in
granulomatous in ammation.
Small Granular KPs Also known as They are composed of lymphocytes, and are characteristic of
non-granulomatous uveitis.
Red KPs omposed of R s and in ammatory cells. Seen in haemorrhagic uveitis.
Old KPs In healed uveitis with crenated margins.

Fig.10.5: Mutton fat KPs Fig.10.6: Fine KPs

• Iris Nodules: features of granulo-matous inflammation .

Koeppe nodule: At the pupillary border.
Busacca nodule: At the base of the iris.

Fig.10.7: Busaca Fig.10.8: Koeppe

220 | Ophthalmology
• Aqueous cells: Sign of active inflammation. They may settle in anterior chamber as
hypopyon (sterile)

Fig.10.9 (a): cells in anterior chamber Fig.10.9 (b): Hypopyon

• ueous are Due to leakage of proteins from the inflamed capillaries of the iris
and pars plicata. It is based on Tyndal phenomenon/Brownian movements.
• Posterior Synechiae

Fig.10.10: Seclusio pupillae

Posterior synechiae extending 360 causing papillary block.

↓
Iris bombe
↓
PAS (Peripheral anterior synechiae leading to raised intraocular pressure due to angle
closure.)
Occlusio papillae: Obstruction of aqueous flow due to organi ation of exudates across
the entire pupil which block the pupil, also known as blocked pupil.
• Anterior vitreous cells.
• Pupil constricted. If posterior synechiae, irregular and constricted pupil, called
Festoon-shaped Pupil. Sluggish pupillary reaction.

Treatment:
Steroids: Topical
Mydriatics with strong cycloplegic action (Atropine).
 a| 221
Intermediate Uveitis or Pars Planitis
Primary
diopathic, insidious, chronic, intra-ocular inflammation typically affecting children or
young adults.

Secondary:
• Sarcoidosis
• Retinitis pigmentosa
• Multiple sclerosis
• TB, syphilis, Lyme’s disease, toxocara

Clinical features:
• Floaters
• Diminished vision- if associated with Cystoid macular edema
• Vitritis: Cells, Snow balls or cotton balls. Mild peripheral periphlebitis. Sheathing of
terminal venules (Snow – Banking): Hallmark of pars planitis.

Fig.10.11:

Complications:
• CME.
• Secondary cataract.
• Tractional RD.
• Cyclitic membranes.

Treatment:
It is four step approach.
• Periocular steroid injections.
• Systemic steroid and cytotoxic drugs.
• Cryotherapy of vitreous base.
• Vitrectomy
222 | Ophthalmology
Posterior Uveitis:
t is the inflammation of the choroid along with associated structures i.e. vitreous, optic
disc, macula, peripheral retina and retinal veins. It is usually insidious in nature.

Clinical features:
• Choroiditis: It is seen as round yellowish patches.
• Cystoid macular edema: CME.
• Vitritis
• Papillitis
• Retinal edema
• Periphlebitis
There is no pain, photophobia, lacrimation or circumcorneal congestion.
Most common cause of posterior uveitis is Toxoplasmosis

Treatment:
• Local steroids: Sub-tenon injections of triamicilone acetate.
• Systemic steroids.

Complications of Uveitis:
In the Cornea Iris Lens In the Globe Posterior Segment
• Sclerosing • Atrophy • Complicated • Secondary • CME
keratouveitis • Rubeosis cataract Glaucoma • RD
• Corneal edema • thisis bulbi. • yclitic membrane
• ullous keratopathy formation
• Disciform keratitis Cilio- Choroidal
• and shaped detachment
keratopathy Hypotony.
• Choroidal
neovascular
membrane
 a| 223
Concept 10.3: Systemic Associations of Uveitis: Arthritis
Learning objectives
• To know about some arthritis related uveitis
• To learn features of different types of uveitis

Time Required
1 reading
st
15 mins
2nd look 5 mins

Uveitis Associated with Arthritis:

Disease Features
Ankylosing Spondylitis associated.
Acute, recurrent non-granulomatous iritis.
Negative RA factor.
Reiters Syndrome Urethritis.
Conjunctivitis.
Sero-negative arthritis
associated.
Psoriatic Arthritis Sero-negative arthritis.
associated
Conjunctivitis.
Acute iritis.
Keratitis.
Secondary s ogren s syndrome
Juvenile Chronic Arthritis hildren below age of years Sero negative arthritis.
Divided into 3 types:
Systemic onset
Polyarticular (> 5 joints involved)
Pauciarticular (< 5 joints involved)
Uveitis is commonest in Pauciarticular JCA.
hronic non granulomatous, bilateral anterior uveitis.
Also called “White Uveitis"
224 | Ophthalmology
Concept 10.4: Systemic Associations of Uveitis: Infections
Learning objectives
• To know about some infections associated with uveitis
• To learn features of different types of uveitis

Time Required
1 reading
st
20 mins
2nd look 5 mins

Systemic Associations of Uveitis: Infections

Disease Main Uveitis Features Treatment
Toxoplasmosis: Iridocyclitis: Granulomatous or non- Systemic steroids
(Most commonly is in foetal granulomatous.
life and later it reoccurs in old Sulphonamide
healed chorio-retinal scar due Posterior Uveitis:
to rupture of cyst) “Headlight in Fog Appearance”. Pyrimethamine

Deep retinitis (involving outer retinal Co-trimoxazole

layer) Clindamycin
Syphilis Acute granulomatous or non- 12-24 MU of aqueous penicillin
granulomatous panuveitis I/V for
Iris Roseola days followed by .
Unifocal choroiditis I/M for 3 weeks.
Other important feature –
“Salt and pepper fundus”
rgyll Robertson pupil
Tuberculosis Chronic granulomatous panuveitis ATT Drugs.

Chronic iridocyclitis:
Most frequent feature
Choroditis: Focal or multifocal.
Retinal vasculitis.
Moderate vitritis.
Severe ischemic periphlebitis.
eripheral capillary closure
neovascularisation.
 a| 225

AIDS CMV Retinitis: It is the most I/V Gancyclovir.

(Retinal Microangiopathy common opportunist ocular infection I/V Foscarnet.
is the most common of AIDS - Sauce and Cheese Intravitreal Gancyclovir
ocular manifestation of Retinopathy” implants
HIV infection -Cotton-
wool spots, haemorrhages, Varicella- Zoster Retinitis: It causes
microaneurysms) Acute Retinal Necrosis

Cryptococcal and Histoplasmal

Choroiditis
Leprosy Acute iritis: It occurs due to
(Ocular involvement is more deposition of immune complexes in
in lepromatous leprosy than in the anterior uvea.
tuberculoid leprosy Chronic uveitis: It occurs due
to direct invasion of the bacilli.
The pathognomic feature is IRIS
PEARLS. These are histiocytes
containing bacilli arranged along
the pupillary border. t resembles a
necklace.
River Blindness Chorio-retinitis: Chronic, non- Ivermectin:
(Onchocerciasis) granulomatous Given only to those at high risk
of blindness because treatment
can lead to severe, acute,
systemic, in ammation called
SR that
can cause death.

Fig.10.12: Toxoplasmosis Fig.10.13: Cytomegalo retinitis

226 | Ophthalmology
Concept 10.5: Other Systemic Associations of Uveitis
Learning objectives
• To know about some infections associated with uveitis
• To learn features of different types of uveitis

Time Required
1 reading
st
50 mins
2nd look 20 mins

Sarcoidosis:
It is an idiopathic, multisystem disorder characterised by presence of non-caseating
granulomata in lungs and other organs.

Ocular features:
Adnexa Granuloma conjunctiva, episclera, sclera.
KCS- due to involvement of lacrimal gland
Anterior uveitis Chronic granulomatous iridocyclitis
Iris nodules
Fundus Changes eriphlebitis dvanced stage of vascular sheathing leads to andle wax
drippings.
Pre-retinal nodules- Lander’s sign
Snow ball opacities in vitreous
Disc granuloma
Optic atrophy

Fig.10.14: Periphlebitis in sarcoidosis Fig.10.15: Sarcoidosis

Behcet’s Disease:
diopathic multisystem disorder, affecting young men leading to obliterative vasculitis
due to circulating immune complexes.
 a| 227
Clinical Features:
• Oral ulceration.
• Recurrent genital ulceration.
• Skin lesions: Erythema nodosum
• Positive pathergy test.
• HLA- B5 associated.
• Eye involvement- Severe bilateral nongranulomatous panuveitis (Acute recurrent
iridiocyclitis with transient hypopyon, retinitis, vitritis, vasculitis)

Vogt- Koyanagi- Harada Syndrome [VKH]:

diopathic multisystem disorder which typically affects pigmented individuals.

HLA-DR4 associated.
Skin and Hair Neurological Features: Auditory Ocular Features
Changes: symptoms
Alopecia Meningeal Irritation Tinnitus ilateral granulomatous panuveitis
Poliosis Encephalopathy Vertigo alen uchs nodules in ammatory cells
Vitiligo CSF- Lymphocytosis Deafness. in R and ruch s membrane
(Suguiras sign) Pigment epithelial atrophy (sunset glow
fundus)
Multifocal choroiditis and exudative RD

Fig.10.16: Vogt–Koyanagi–Harada syndrome

228 | Ophthalmology
Sympathetic Ophthalmitis:
• Bilateral, granulomatous panuveitis.
• Occurs after accidental penetrating trauma.
• Traumatized eye is the exciting eye and the fellow eye is sympathizing eye.
• 65% of cases occur between 2 weeks and 3 months after injury.
• 0 of cases occur within first year.
Blurring of vision due to loss of accommodation- 1st symptom
etrolental flare: 1st sign
Ocular Signs – similar to VKH syndrome but with sparing of choriocapillaries and absence
of systemic features

Treatment:
• Vigorous steroid therapy by all possible routes of administration.
• Immunosuppressive therapy: with chlorambucil, cyclophosphamide or cyclosporin, in
severe steroid – resistant cases.
• Enucleation- within 2 weeks of injury will prevent sympathetic uveitis

Fig.10.17: SYMPATHETIC OPHTHALMITIS

Ophthalmia Nodosum
Severe, granulomatous iridocyclitis with nodule formation, due to caterpillar hair inside
the eye

Eales Disease (Periphlebitis Retinae):

ainly affects young males. B/ , idiopathic

Etiology:
• Idiopathic.
• Hypersensitivity to tuberculo protein leads to peripheral retinal vasculitis.
 a| 229
Presentation:
• Sudden blurring of vision with floaters as a result of vitreous haemorrhage.
• Sheathing of small peripheral retinal veins.
• Massive proliferative retinopathy Vitreous or retinal haemorrhage TRD.

Treatment:
1. PRP
2. Pars plana vitrectomy

Specific u eitis s n omes

Posner Schlossman Syndrome: Fuch’s Uveitis Syndrome or
Glaucomatocyclitic crisis Fuch’s Heterochromic Cyclitis
Young patient Middle age patient
Non-granulomatous, anterior uveitis Non-granulomatous, anterior uveitis
possibly cytomegalovirus
(CMV) or H. pylori may play a role
cute blurring of vision and halos symptomatic, sometimes with blurring of vision
Few depigmented KPs Heterochromia iridis
No posterior synechiae Iris atrophy
IOP-: 40-60mmHg No posterior synechiae
Gonioscopy shows open angles. Keratic precipitates- small, stellate and grey- coloured;
Optic nerve – No cupping Rubeosis fine msler s sign acute
isual field is normal. hyphema following ocular decompression such as paracentesis

Complications:
Cataract.
Glaucoma – usually of open- angle type

Treatment for both:

Topical steroids with anti-glaucoma drugs to decrease the IOP.

Fig.10.18: FUCH’S HETEROCHROMIC Fig.10.19: Amsler sign

IRIDOCYCLITIS
230 | Ophthalmology
Endophthalmitis:
It is an inflammation of the inner eye fluids and tissues ie uveal tissue, retina, vitreous
humor and aqueous humor.
Outer coat ie sclera is spared.
Most common cause of endophthalmitis is intraocular surgery.
It may also occur after a penetrating trauma, entry of the microbes endogenously or by
metastatic spread.

Organisms:
Exogenous endophthalmitis:
• Post-operative: Acute post-operative ie within 7 days after surgery: Staphylococcus
epidermidis, Staphylococcus aureus, Streptococcus. Delayed onset i.e. from a week
to months after surgery: Fungi, P. acne (most common).
• Post traumatic: Bacillus, Staphylococcus epidermidis, Fungi, Streptococcus.
Endogenous endophthalmitis: Bacillus cereus (drug abusers), Staphylococcus aureus,
Streptococcus, Haemophilus in- fluen ae, meningococci etc.

Clinical features:
• Severe ocular pain.
• Redness.
• Lacrimation.
• Photophobia and marked loss of vision.
• Swollen lids.
• Chemosis of conjunctiva.
• Conjunctival and circumcorneal congestion.
• Hypopyon.
• Corneal edema.
• Amourotic cat’s eye reflex.

Treatment:
Intravitreal antibiotics
Topical and systemic steroids
Pars plana vitrectomy

Panophthalmitis:
nflammation of all the structures of the eye

Complications include:
• Orbital cellulitis.
• Cavernous sinus thrombosis.
• Meningitis.
• Encephalitis.

Treatment:
Eviseration
Systemic antibiotics
 a| 231
Worksheet
• DO THIS CHAPTER FROM DQB

• EXTRA POINTS FROM DQB


232 | Ophthalmology
• Identify

• Name the KPs whose description is given

Large and are composed of epitheloid cells and macrophages. Seen in
granulomatous in ammation.
Also known as They are composed of lymphocytes, and are characteristic of
non-granulomatous uveitis.
omposed of R s and in ammatory cells. Seen in haemorrhagic uveitis.
In healed uveitis with crenated margins.

• Write features of
Reiters Syndrome ______________

Ocular Features of VKH syndrome

• Name the iris nodules? _______________________

 a| 233
• The most common ocular manifestation of HIV infection -______________
• Acute hyphema following ocular decompression such as paracentesis in Fuch’s uveitis
is _________________
• Endophthalmitis is inflammation of -

Write some features of Bechets disease

• Sympathetic Ophthalmitis:

Critical period of development is _______________

1st symptom in sympathising eye - ___________

1st sign in sympathising eye - ___________

• Identify the organism causing it

234 | Ophthalmology
EXTRA POINTS:
11 Squint

CONCEPTS
 Concept 11.1 Extraocular muscles and actions

 oncept uint e nition and tests

 Concept 11.3 Concomitant vs Inconcomitant

squint

 Concept 11.4 Tests for binocular vision

236 | Ophthalmology
Concept 11.1: Extraocular muscles and actions
Learning objectives
• To know about extrocular muscles, their origin, insertion and actions
• To learn about laws governing extraocular muscles

Time Required
1 reading
st
40 mins
2nd look 20 mins

EXTRAOCULAR MUSCLES

Fig.11.1: Actions, Origin and insertion of extraocular muscles

 nt| 237

Muscle Primary Secondary Tertiary Origin Insertion

Medial rectus Adduction - - Annulus of Zinnn Anterior sclera (5.5 mm)
Lateral rectus Adduction - - Annulus of Zinnn Anterior sclera (7 mm)
Inferior rectus Depression Extorsion Adduction Annulus of Zinnn Anterior sclera (6.5 mm)
Superior rectus Elevation Intorsion Adduction Annulus of Zinnn Anterior sclera (7.5 mm)
Inferior oblique Extorsion Elevation Adduction Body of maxilla Posterior sclera
Superior oblique Intorsion Depression Adduction Body of sphenoid Posterior sclera
The number in bracket is distance of muscle insertion from limbus
Superiors are intorters
Recti are adductors
• The vertical recti run in line with the orbital axis and are inserted in front of the
equator. They therefore form an angle of 23° with the visual axis
• The obliques are inserted behind the equator and form an angle of 51° with the visual
axis

GAZE POSITIONS

Fig.11.2:

Hering’s law: It states that during any conjugate eye movement, equal and simultaneous
innervation flows to the yolk muscles.
Sherrington’s Law of reciprocal innervations: It states that increased innervation
and contraction of a muscle is automatically associated with a reciprocal decrease in
innervations and relaxation of its antagonists.
Primary position of gaze: Position of eyes in binocular vision when, with the head
erect, the object of regard is at infinity and lies at intersection of saggital plane of the
head and horizontal plane passing through the centre of rotation of the two eye balls.
Secondary position: Supreversion, Infraversion, Levoversion, Dextroversion.
Tertiary position: Vertical + Horizontal position i.e. dextroelevation, Levoelevation,
dextrodepression, Levodepression.
238 | Ophthalmology
oncept S uint efinition an tests
Learning objectives
• To know about types of squint
• To learn various tests to determine squint

Time Required
1 reading
st
50 mins
2nd look 25 mins

The misalignment of the visual axis of the two eyes is known as squint or strabismus.
Strabismus is classified as:
atent squint Phorias : t is further classified as exophoria, esophoria, hypophoria or
hyperphoria.
anifest squint Tropias : t can be classified as: Esotropia, Exotropia, Hypeotropia or
Hypertropia

Fig.11.3:

Tests for Squint:

Hirschberg Test: Deviation of the corneal light reflex from the centre of the pupil.
eflex at the inner border of the pupil indicates squint of 15 .
eflex at the centre of the inner and outer border of the pupil indicates a squint of 0
degrees.
eflex at the limbus indicates squint of 5 .
 nt| 239
In general, for every 1 mm that the light is decentered, the eye is turned about 15 prism
diopters (7 degrees from center).

Fig.11.4:

Cover-uncover test:
• Cover component:
Detects heterotropias
Cover straight eye
Look at uncovered deviated eye (movement indicates tropia)
• Uncover component:
Detects heterophorias
Uncover straight eye
ook at uncovered eye for deviation and refixation movement indicates phoria in this
eye)
Alternate –Cover Test: In this test we alternate cover both the eyes with the cover
and see the movement of the uncovered eye.
240 | Ophthalmology
COVER TEST FOR TROPIAS

Fig.11.5:
 nt| 241
COVER-UNCOVER TEST FOR PHORI
AS/LATENT SQUINT

Fig.11.6:

Krimky’s test/Prism bar test: Prisms of increasing power are placed in front of
deviated eye till the eye appears straight or light reflex is aligned straight. t measures
heterotropias. [Light rays are deviated towards the base of the prism, and the objects
appear displaced towards the apex].

Fig.11.7: PRISM BARS

242 | Ophthalmology

Fig.11.8: PRISM BAR COVER TEST

Alternate prism cover test: Measures total deviation (heterotropias and phorias).
Prism over deviated eye and alternate cover each eye until no movement is seen.
Maddox rod and Maddox wing are used to assess the latent squint.
n addox wing -Dissociates two eyes for near fixation
n addox rod - Dissociates two eyes for distance fixation. t consists of series of fused
high power cylinder red rods.

Fig.11.9:
 nt| 243
Concept 11.3: Concomitant vs Inconcomitant squint
Learning objectives
• To know about types of squint
• To learn various tests to determine squint

Time Required
1 reading
st
60 mins
2nd look 25 mins

Concomitant vs Inconcomitant [Paralytic squint]

• Non-Paralytic/Concomitant- Primary deviation is equal to secondary deviation.
Primary deviation is the deviation of the squinted eye, whereas secondary deviation
is the deviation of the normal eye.
• Paralytic/Incomitant- Secondary deviation is more than the primary deviation.
This is due to Herring’s Law.

Features of Paralytic squint:

ƒ Diplopia.
ƒ Confusion.
ƒ Nausea and vertigo.
ƒ Ocular deviation.

Diplopia (Double Vision):

Horizontal – Images are side by side.
Vertical – Images are up and down.
Torsional - oblique

Horizontal Diplopia may be:

ƒ Uncrossed: When the false image is on the same side as the deviating eye.
ƒ Crossed – When false image is on opposite side of deviating eye.

Convergent Squint: Uncrossed diplopia

Divergent Squint: Crossed diplopia
Uniocular Diplopia: Causes:
ƒ Subluxated lens.
ƒ Double pupil.
ƒ Incipient cataract.
ƒ Keratoconus.

Binocular Diplopia: Causes:

ƒ Paralytic squint.
ƒ Restrictive squint.
ƒ Anisometropic glasses- (uniocular aphakic glass).
ƒ After squint correction
244 | Ophthalmology
Third Nerve Palsy:
ƒ Ptosis.
ƒ Eye is - Down and Out.
ƒ Defective – adduction, elevation and depression.
ƒ Dilated pupil with defective accommodation.
ebino: all-Eyed Bilateral nternu- clear Ophthalmoplegia . Due to lesions involving
paired medial rectus subnuclei. Defective convergence and adduction.
Benedickt’s Syndrome : psilateral third nerve palsy and contralateral hemitremor.
Weber’s Syndrome: Ipsilateral third nerve palsy and a contralateral hemiparesis.

Fig.11.10: Left 3rd nerve palsy

Fourth Nerve Palsy:

• Hyperdeviation.
• Excyclotorsion: Compensated by head tilt to opposite shoulder.
• Limited depression in adduction.
• Diplopia: Vertical. Worse on looking down
Bielchowsky’s sign: Increase of the hyperdeviation on tilting the head to the ipsilateral
shoulder. This is a feature of fourth nerve palsy.

Fig.11.11: Left 4th nerve palsy

Sixth Nerve Palsy:

• Defective abduction.
• Convergent strabismus.
• Horizontal diplopia.
• Face turn into field of action of paralysed muscle
 nt| 245
Millard Gubler Syndrome : Ipsilateral sixth nerve palsy with contralateral hemiplegia.

Fig.11.12: Left 6th nerve palsy

Concomitant squint
Concomitant esotropia:
• Infantile esotropia- Presents at 6 months of birth arge angle 0 prism
D .Alternating fixation in primary position but cross
• Accomodative esotropia- Refractive- corrected by spectacles. Non refractive- high
AC/A ratio (accommodative convergence/accommodation_- corrected by bifocals.
Mixed- components of both
• Sensory esotropia (disruption of binocular single vision in children e.g. congenital
cataract)
• Consecutive esotropia (after correction for exotropia)

Concomitant exotropia:
• Infantile exotropia- Present at birth, large and constant angle
• Intermittent exotropia- Convergence insu ciency worse for near, needs resection
or recess-resect). Divergence excess (worse for distance, needs LR recession):
• Sensory exotropia (disruption of binocular single vision in children e.g. congenital
cataract)
• Consecutive exotropia (after correction for esotropia)

Treatment :
Incomitant/Paralytic Squint:
Wait for 5-6 months, if no improvement do surgery.[For an underacting muscle we do
resection and for a overacting muscle we do recession].

Concomitant Squint / No-Paralytic squint:

Sequence of management is as follows:
efraction Occlusion Orthoptic Excercises Surgery

Fig.11.13: ORTHOPTICS: EXCERCISES

246 | Ophthalmology
Concept 11.4: Tests for binocular vision
Learning objectives
• To know about different tests to evaluate binocularity and stereopsis

Time Required
1st reading 40 mins
2 look
nd
15 mins

The synoptophore
Test of Binocular single vision
t dissociates two eyes for both near and distance fixation

Fig.11.14: SYNAPTOPHORE

Binocular Vision:
Defined as that state of simultaneous vision with two seeing eyes that occurs when
an individual fixes his visual attention on an object of regard. t is assessed by a
synaptophore.

Grades:
I – Grade- Simultaneous perception
II- Grade – Fusion.
III- Grade – Stereopsis

Horopter:
It is the sum total of points in physical space; that stimulate corresponding retinal
elements of the two eyes.
Panum’s Area:
The field in front of and behind the horopter in which the expected diplopia does not
occur is known as “Panums fusional space”.
 nt| 247
isual reflex fixation in infants starts developing at 6 weeks of age and develops fully
till month of age.
Binocular function fully develops by 6 years and orthoptic exercises are most useful till
8-9 years of age.
Visual acuity is a measure of form sense.

Fig.11.15: SIMULTANEOUS PERCEPTION

Fig.11.16: FUSION
248 | Ophthalmology

Fig.11.17: STEREOPSIS

OTHER TESTS FOR STEREOPSIS

TITMUS STEREO TEST:
FLY TEST, ANIMAL TEST & CIRCLES TEST

Fig.11.18:
 nt| 249

Fig.11.19: Randot E Fig.11.20: TNO

Fig.11.21: Lang Fig.11.22: Frishy

Fig.11.23: WORTH FOUR DOT TEST

250 | Ophthalmology
Tests binocular vision and suppression
a. Shown to patient
b. f lights are seen, indicates normal fusion
c. If 2 lights are seen, indicates left suppression
d. If 3 lights are seen, indicates right suppression
e. If 5 lights are seen, indicates diplopia

Fig.11.24: Bagolini striated glasses

Tests binocular vision and suppression

 nt| 251
Worksheet
• DO TH S CHAPTE F O D B

• E T A PO NTS F O D B


252 | Ophthalmology

Muscle Origin Insertion Primary action

Superior rectus
Inferior rectus
Superior oblique
Medial rectus

• The obliques are inserted behind the equator and form an angle of ____ with the
visual axis

• Write the diagnosis for each

 nt| 253
• What test is being done?

• If the patient is normal, he will _________ from right eye and _______ from left eye

• Uniocular Diplopia: Causes:

254 | Ophthalmology
• The test is used for? ___________

• Convergent Squint: ____________diplopia

• Divergent Squint: ____________diplopia

• Name the nerve involved here _______________________

• Write the features of the diagnosis

 nt| 255

• Identify the device

• What does c and d indicate here?

256 | Ophthalmology
EXTRA POINTS:
12 Optics

CONCEPTS
 Concept 12.1 Basics

 Concept 12.2 Visual acuity charts

 Concept 12.3 Slit lamp and Ophthalmoscopes

 Concept 12.4 Errors of Refraction

 Concept 12.5 Pin hole and macular function tests

 Concept 12.6 Amblyopia

 Concept 12.7 Retinoscopy

 Concept 12.8 Refractive procedures

258 | Ophthalmology

Concept 12.1: Basics

Learning objectives
• To know basic points regarding slit refractive power and index of eye
• To know about visual angles
• To learn about Purkinje images

Time Required
1st reading 20 mins
2 look
nd
5 mins

• Total diopteric power of eye is 58 D to 60 D.

• educed eye: Simplified optics of eye is referred as reduced eye.
• Refractive power of the cornea is 44D
• Refractive power of the lens is:16D-17D
• Refractive index of the cornea is 1.376.
• Refractive index of lens is 1.386-1.406.
• Refractive index of aqueous and vitreous humor is 1.33

Visual angles:
a. Angle Alpha ( ):
Angle between optical axis and visual axis at the nodal point.
b. Angle Gamma ( ):
Angle between optical axis and fixation axis at the centre of rotation of the eyeball.
c. Angle Kappa ( ):
Angle between visual axis and pupillary line at cornea

Fig.12.1:
 Opt | 259
Positive angle kappa – Pseudo exotropia. It is a feature of hypermetropia.
Negative angle kappa- Pseudo esotropia. It is a feature of myopia.

Purkinje image:
Formed when strong beam of light is projected on eye.
• Ist and IInd image- by anterior and posterior surface of cornea.
• IIIrd and IVth image- by anterior and posterior surface of lens.
• IVth image- is inverted.
In aphakia, 2 images are absent (3rd and 4th).
In pseudophakia, 4 images

Fig.12.2:
260 | Ophthalmology

Concept 12.2: Visual acuity charts

Learning objectives
• To know about different vision testing charts

Time Required
1 reading
st
30 mins
2 look
nd
10 mins

Visual acuity measurement by Snellen chart

etters are made of different si es and designated by distance at which letter subtends
5 min of ARC, e.g. letters on 6/6 line subtend 5 min of ARC when viewed at 6m, each
part (stroke) of the letter subtends 1 min of arc. It measures minimum resolvable visual
acuity. In Normals, the minimum resolvable angle is 30 s to 1 min of arc.

Fig.12.3: Snellen chart

Snellen chart
Near visual acuity is assessed commonly at 0 cm, using charts with different si e print
samples. Jaeger, Snellen are examples.
 Opt | 261

Fig.12.4: Near vision chart

Fig.12.5: Landolt C chart

Landolt C chart chart is a way to check vision for illiterate or mute patients.
262 | Ophthalmology
ETDRS chart (Early Treatment of Diabetic Retinopathy Study Chart)

Fig.12.6:

Same number of letters per row five letters per row . hen using a og A chart, visual
acuity is scored with reference to the logarithm of the minimum angle of resolution. It
is done at 4 m.
Vision testing in infant: The pattern visual evoked potential (VEP) and preferential
looking behaviour by Teller chart. An objective measure of the visual acuity may also be
made by utili ing the phenomenon of opticokineticnystagmus.

Fig.12.7: Opticokineticnystagmus drum

 Opt | 263
Other charts used in children:
ardiff acuit cards for children 2–4 years of age.

ea ure testin in a young child. The child matches the presented figure. The child
points to one of four choices to match the figure or letter he or she sees on the computer
monitor or chart in the distance.

HOTV acuity testing. The child is asked to match the indicated letter on the chart with
a hand-held card displaying the HOTV letters.

STYCAR (sight testing for young children and retards)

264 | Ophthalmology

Concept 12.3: Slit lamp and Ophthalmoscopes

Learning objectives
• To know basic points regarding slit lamp and ophthalmoscopes with lenses used

Time Required
1 reading
st
20 mins
2 look
nd
5 mins

Fig.12.8: SLIT LAMP

SLIT LAMP
The slit-lamp is essential for a thorough examination of the eye. The magnification can
be varied by changing the power of the eye pieces and the objective lens. It can view
upto anterior 1/3rd of vitreous. Coupled with additional lens, fundus and optic disc can
also be seen (slit lamp biomicroscopy)
For an emmetropic, magnification of Direct ophthalmoscope is 15 times, image formed
is virtual and erect and is used to see central retina.
agnification of ndirect ophthalmoscope with 20D lens is times, image formed is real
and inverted and is used to see the periphery of the retina.
 Opt | 265

Fig.12.9: DIRECT OPHTHALMOSCOPE Fig.12.10: INDIRECT OPHTHALMOSCOPE

Fig.12.11: 20D – FOR INDIRECT OPHTHALMOSCOPY

90D/78D – FOR SLIT LAMP
BIOMICROSCOPY
266 | Ophthalmology

Concept 12.4: Errors of Refraction

Learning objectives
• To know about various errors of refraction
• To learn about presbyopia

Time Required
1 reading
st
40 mins
2 look
nd
15 mins

Errors of Refraction:
Myopia:
It is a refractive error where the light rays are focused in front of the retina. It is
corrected by using concave lens. Any myopia of more than 6D is called high myopia.
yopia with fundus changes is called pathological myopia.
Far Point and Near Point Come Nearer in yopia.

Hypermetropia:
It is a refractive error where the light rays are focused behind the retina. It is corrected
by convex lenses.
The fundus changes are:
• Pseudopapillitis.
• Silk shot appearance.
• Degenerative retinoschisis.
Near Point Becomes Distant in Hypermeropia.

Refractive Error

Fig.12.12:
 Opt | 267
Astigmatism:
hen the refractive power in the two principal axis of the eye is different, it is called
astigmatism. It is corrected by cylindrical lenses.
It can be due to corneal curvature abnormality, lenticular curvature abnormality/oblique
position of lens and oblique displacement of macula.

Fig.12.13:

pes of asti matism can e classifie in i e ent a s

Simple myopic Regular With the rule astigmatism – vertical axis (90 Corneal
(refractive degree) is steeper
Simple power change Lenticular
hypermetropic regularly Against the rule astigmatism – horizontal axis
from one (0/180 degree) is steeper
meridian to Retinal
Compound other)
myopic Oblique – When the 2 mridians are not
horizontal or vertical, but at 90 degress
Compound
hypermetropic Irregular Bioblique - When the 2 mridians are not at 90
(like in degree to each other
keratoconus,
Mixed corneal
opacity)
268 | Ophthalmology

Fig.12.14:

Anisometropia:
hen the total refraction of the two eyes is unequal by 2.5 D.

Aniseikonia:
hen the images projected to the visual cortex from the two retina are abnormally
unequal in si e and/or shape.

Pseudomyopia:
• Due to excessive ciliary muscle tone which causes increase in accommodation leading
to increase in the power of the lens.
• Distant vision is decreased while near vision is good.
• Present in children who try to compensate their refractive error
• Can also be drug induced eg. Cholinergic drugs since it causes ciliary spasm and will
increase the tone of the ciliary muscle.

Aphakia:
Absence of the Lens:
• Eye becomes highly hypermetropic.
• Total power of eye is reduced to + 44 D from + 60 D [less by 16D-17D].
• Total loss of accommodation.
• Best available treatment for aphakia is posterior chamber intraocular lens.

Other methods of correcting aphakia:

• Spectacles.
• Contact lens.
• Refractive surgery:
 Opt | 269
ƒ Keratophakia.
ƒ Epikeratophakia.
ƒ Hyperopic Lasik.

Disadvantages of spectacle correction in aphakia

• Problem of spherical and chromatic aberration
• Prismatic effect of thick lenses
• Roving ring scotoma (Jack in the box phenomenon)
• Field of vision is limited
• Not useful in unilateral aphakia as it causes diplopia

Fig.12.15: Pincushion Distortion

Fig.12.16: Jack in box phenomeon

270 | Ophthalmology
Presbyopia
Presbyopia is when eyes gradually lose the ability to see near things clearly due to
decrease in accommodation with age. It is a normal part of aging. Presbyopia usually
becomes noticeable in your early to mid-40s.

Common symptoms of presbyopia are:

• having eyestrain or headaches after reading or doing close work
• having di culty reading small print
• having fatigue from doing close work

Treatment
Near glasses (plus)
Bifocals (if patient has refractive error for far as well)

Fig.12.17: BIFOCALS

Fig.12.18: BIFOCALS (executive) – preferably in pediatric patients

 Opt | 271

Concept 12.5: Pin hole and macular function tests

Learning objectives
• To know basic points regarding slit lamp and ophthalmoscopes with lenses used

Time Required
1 reading
st
20 mins
2 look
nd
5 mins

PIN-HOLE
Pinhole aperture compensates for the effect of refractive errors, and consists of an
opaque occlude perforated by one or more holes of about 1 mm diameter. If the vision
is subnormal, the visual acuity is again determined by asking the patient to read the
letters through a pinhole. If it improves, it indicates an underlying refractive error.
However, visual acuity in patients with macular disease and posterior lens opacities may
be worse with pin hole.

Fig.12.19:

Macula function tests

272 | Ophthalmology

Fig.12.20: Normal Amsler grid Fig.12.21: Amsler grid with metamorphosia and
positive scotoma
 Opt | 273

Concept 12.6: Amblyopia

Learning objectives
• To know basic points regarding slit lamp and ophthalmoscopes with lenses used

Time Required
1 reading
st
20 mins
2 look
nd
5 mins

Amblyopia:
t is defined as deficiency of form sense resulting in reduction in visual acuity of greater
than two lines between the eyes or an absolute reduction in acuity below 6/9.
Squint is the most common cause of amblyopia.
Pathophysiology: Cell shrinkage in parvocellular layers of lateral geniculate body.

Signs and symptoms:

• Decreased visual acuity.
• Decreased accommodation ability.
• Afferent pupillary defect- in severely affected eye.
• Eccentric viewing.
• Enhanced crowding phenomenon.
• Neutral density filters decrease vision in normal eye and not in amblyopic eye.

Types:
• Strabismic Amblyopia – due to squint
• Form deprivation Amblyopia: congenital cataract, rubella keratitis.
• Refractive Amblyopia:
ƒ Anisometropic Amblyopia.
ƒ Ametropic Amblyopia.
ƒ eridional Amblyopia.

Treatment:
• Refractive correction.
• Occlusion.
• Penalisation (with atropine).
• CA stimulator high contrast square wave gratings of different frequency .
• Pleoptics – Stimulation of fovea by means of after–images in case of eccentric fixation.
• Drug therapy: Levodopa/Carbidopa:
• Occlusion therapy is the mainstay of the treatment in which NO A eye is occluded
274 | Ophthalmology
Concept 12.7: Retinoscopy
Learning objectives
• To know steps of retinoscopy
• To know about refractive error prescription
• To learn basics of contact lenses

Time Required
1 reading
st
40 mins
2 look
nd
15 mins

Retinoscopy
Also called Skiascopy or shadow test, is an objective method of finding out the error of
refraction by the method of neutralisation.

Fig.12.22: Retinoscopes Fig.12.23: Priestley Smith Retinoscope

Observation:
Depending upon the movement of red reflex, when a plane mirror retinoscope is used,
reflex direction is seen like these :

"Against"

Fig.12.24:
 Opt | 275
Plus lens are added if reflex moves in same direction with movement of retinoscope
inus lens are added if reflex moves in opposite direction with movement of retinoscope

Deduction for distance:

If retinoscopy is performed at a distance of 1m, 1D is deducted. If retinoscopy is
performed at a distance of 67cm, 1.5D is deducted.

Deduction of cycloplegic:
Atropine- 1D: <7 yrs of age: Atropine should be used for cycloplegic.
Atropine ointment is the choice of cycloplegic in children. 1% ointment is given 3 times
a day for 3 days.
Homatropine- 0.5D

his is one in t o a is he final p esc iption is i en as e ample

Add is given for near vision if required

If retinoscopy is done from 1 m with no cycloplegia, then the results are interpreted as
below:
• No movement of red reflex indicates myopia of 1 D.
• hen red reflex moves along with the movement of the retinoscope, it indicates
either emmetropia or hypermetropia or myopia of less than 1 dioptre
• Against the movement indicates myopia of more than 1D.

Contact Lens:
Contact lens is a small polymer material designed to rest on the cornea or sclera

Purpose:
• Optical- used to correct refractive errors.
• Therapeutic – Bandage contact lens
• Cosmetic – coloured contact lenses

Types:
aterial:
• Hard- Gas-impermeable –P A Poly methyl methacrylate
• RGP-Rigid gas-permeable –
CAB- Cellulose Acetate Butyrate.
Styrene.
Siloxane- methacrylate.
Fluoro based or fluorinated silicon.
276 | Ophthalmology
• Soft:
Hydrogel- HE A.
Elastomer- Silicon rubber.
• Patients using soft contact lens (if use tap water for cleaning the lens) are at increased
risk of Acanthamoeba Keratitis.
• D - Symbolises oxygen permeability of contact lens where D is diffusion co- e cient
and is solubility co-e cient.
• DK/t: Denotes oxygen transmissibility, where t is the thickness of the contact lens.
• Fluorescein: s not used in soft- lens fitting evaluation as it stains the lens. Except for
large molecules fluorescein like Flourexon.
• Ben alkonium chloride should never be used for disinfecting soft contact lens.
• Toric lenses- For correcting astigmatism, contact lenses with cylindrical power are
called toric lenses.
• X- chrom lenses- These lenses transmit light in red part of the spectrum and are
useful to patients with red-green defective vision.
 Opt | 277

Concept 12.8: Refractive procedures

Learning objectives
• To know some refractive procedures and range of refractive error they can correct
• To know basic of LASIK

Time Required
1 reading
st
40 mins
2 look
nd
15 mins

REFRACTORY PROCEDURES
Procedure Detail Range
Radial keratotomy Linear radial incisions (80% depth) are made in Upto - 6 D
peripheral cornea sparing a central optic zone
thereby attening it
Intracorneal rings or inserted in a paracentral corneal stromal pocket Upto - 6 D
segments lead to central attening
Photorefractive keratotomy xcimer laser ablation of the superficial layer of Upto -4D
(PRK) the cornea, after removing the epithelium. Astigmatism up to
around 3 D and low–
moderate hypermetropia
Laser assisted epithelial Resembles excimer laser PRK with an epithelial
keratomileusis (LASEK) ap.
Laser-assisted in situ Excimer laser beam reshapes the cornea by +4 to -12D
keratomileusis (LASIK) ablating the superficial stroma to a predetermined astigmatism up to 5 D
extent after lifting a ap of the cornea with a
sharp
Microkeratome or femtosecond laser
Refractive lenticule Refractive lenticule extraction (ReLEx) uses a +4 to -12D
extraction (SMILE) femtosecond laser to cut a lens-shaped piece of astigmatism up to 5 D
corneal tissue (a lenticule) within the intact
cornea. This is then removed a minimally
invasive 4 mm incision (small incision lenticule
extraction – SMILE).

Clear lens extraction -15D

Phakic intraocular lens Concave intraocular lenses of appropriate power +10 to -20D
are fitted in the anterior chamber or posterior
chamber anterior to the natural
crystalline lens.
Holmium:YAG laser or conductive thermokeratoplasty is suitable for lower hyperopia of
11 D to 12.5 D
278 | Ophthalmology

Fig.12.25: Refractive lenticule extraction (SMILE)

Fig.12.26:
 Opt | 279
PHOTOREFRACTIVE KERATECTOMY
Laser epithelial keratomileusis

Fig.12.27: PHAKIC IOLs

280 | Ophthalmology
Worksheet
• DO TH S CHAPTE F O D B

• E T A PO NTS F O D B


 Opt | 281
• Write the diagnosis of each

Refractive Error

• What is the refractive error

• This vision chart is tested from _____m?

282 | Ophthalmology
• Identify the device

• Aniseikonia is __________________________
• Identify the spectacles

• lens are added if reflex moves in same direction with movement of retinoscope
• This chart is used for ___________________
 Opt | 283

Laser-assisted in situ keratomileusis (LASIK) Range? _______________

• hich laser is used in this step of AS

284 | Ophthalmology
EXTRA POINTS: