Clarendonz’16
III YEAR MBBS QUESTION BANK
OPHTHALMOLOGY & ENT
(Short answers)
Best wishes
CLARENDONZ’16 TVMC
UPDATED BY TNMSA ACADEMIC WING
CLARENZ’ 16 Ophthalmology TVMC
1. Daily Requirements and Dietary Source of Vitamin A
900 micrograms for adult male
700 micrograms for adult female
Sources - Carrot, Papaya, Green leafy Vegetables, Drumsticks
2. Two Causes for Ptosis
Neurogenic Ptosis - 3rd Nerve palsy, Horner’s Syndrome, Multiple Sclerosis
Myogenic Ptosis – Myasthenia Gravis, Dystrophica Myotonica, Ocular Myopathy
Aponeurotic Ptosis – Senile Ptosis, Post operative Ptosis
Mechanical Ptosis – Lid Tumors, Multiple Chalazia
3. Two Risk factors for ROP
Low gestation age
Low birth weight
Supplemental oxygen therapy
4. Two Causes for Ambylopia
Visual deprivation as occurs in anisometropia
Light deprivation due to congenital cataract
Abnormal binocular interaction as in strabismus
5. Two Causes for Roth’s spots
Infective Endocarditis
Collagen vascular diseases
Diabetic Retinopathy
Hypertensive Retinopathy
Leukemia
Pre eclampsia
6. Two tests for colour vision
Pseudo isochromatic charts * Holmgren’s Wools test
Edridge Green Lantern test. * Nagel’s Anomaloscope
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7. Two Anti fungal drugs
Topical – Natamycin (5%) , Amphotericin B (10-1.25 mg/ml), Fluconazole (0.2%)
Systemic – T. Fluconazole, T. Ketoconazole
8. Clinical Features of Retinitis Pigmentosa
Visual Symptoms – Night blindness, Tubular vision
Fundus – Retinal Pigmentary changes, Attenuated Retinal arterioles, pale optic disc
Choroidal Sclerosis, cystoid macular edema, cellophane maculopathy
9. Two indications for Paracentesis
Acute angle closure Glaucoma
Central Retinal Artery Occlusion
10. Types of Central Venous Occlusion
Non ischemic CRVO or venous stasis Retinopathy
Ischemic CRVO or Hemorrhagic Retinopathy
11. Two investigations for Intra Ocular Foreign Body
Slit lamp examination with gonioscopy
Plain X ray orbit
Limbal ring localisation
Ultrasonographic localisation
12. Two Differences between Paralytic and Concomitant squint
Paralytic squint – Sudden onset
Diplopia (+)
Ocular movements limited in the direction of paralysed muscle
False projection (+)
Concomitant Squint – Slow onset
Diplopia (–)
Ocular movements full
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False projection (–)
13. Two tests to evaluate vision in children
Dot visual acuity
Miniature toy test
Coin test
Marble game test
14. Two treatment modalities for posterior capsule opacification
In children Anterior vitrectomy and posterior capsulotomy
In adults Nd:YAG laser posterior capsulotomy
15. Action and Nerve Supply of lateral rectus
Action – Abduction
Nerve supply – Abducent Nerve
16. Two uses of ultra sound in ophthalmology
A scan :
(i) Measurement of Axial length
(ii) Anterior chamber depth and Intra Ocular distance
(iii) Thickness of Intra Ocular mass
B scan :
(i) Assessment of posterior segment in presence of opaque media
(ii) Study of Intra Ocular tumors, orbital tumors, other mass lesions
(iii) Localisation of intraocular and Intra orbital foreign bodies
17. Two syndromes associated with Retinitis Pigmentosa
Lawrence Moon Biedl Syndrome
Cockayne’s syndrome
Refsum’s syndrome
Usher’s syndrome
Hallgren’s syndrome
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18. Two types of Surgery for Glaucoma
Laser peripheral iridotomy
Trabeculectomy
Filtration surgery
Prophylactic laser iridotomy
19. Two types of lenses to visualise retina
Hruby lens
78 D lens
90 D lens
Volk lens
20. Two Causes for Axial Proptosis
Intra conal masses
Thyroid Associated Ophthalmopathy
Optic nerve glioma
Cavernous hemangioma
21. Two Differences between corneal ulcer and opacity
Corneal ulcer –
(i) Discontinuation in the normal epithelial surface of cornea
(ii) They may be of Infective, allergic, trophic, peripheral Ulcerative types
(iii) Only the epithelium is involved, other layers are intact
(iv) Topical antibiotics are the main line of treatment
Corneal opacity –
(i) Loss of transparency of cornea due to scarring
(ii) Nebula, Macula, Leukomatous are the major types
(iii) Stromal involvement is predominantly seen in opacity
(iv) Optical iridectomy and keratoplasty are the main line of management
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22. Two complications of acute dacryocystitis
Acute conjunctivitis
Corneal abrasion and ulceration
Lid abscess
Osteomyelitis of lacrimal bone
Orbital Cellulitis
Facial Cellulitis
Acute ethmoiditis
23. Two Causes of Nyctalopia
Vitamin A Deficiency
Tapetoretinal degeneration
Congenital high myopia
Familial congenital night blindness
Oguchi’s disease
24. Two systemic diseases associated with Scleritis
Autoimmune Collagen disorders – RA, Wegener’s granulomatosis, SLE, PAN
Metabolic disorders – Thyrotoxicosis, gout
Granulomatous disease – TB, syphilis, sarcoidosis, leprosy
25. Nerve supply and action of Superior oblique
Nerve supply – Trochlear Nerve
Action –
(i) Primary action – Intorsion
(ii) Secondary action – Depression
(iii) Tertiary action – Abduction
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26. Retinitis Pigmentosa - Fundus findings
Retinal Pigmentary changes – typically perivascular and resemble bone corpuscles
Attenuated Retinal arterioles
Pale optic disc
Choroidal Sclerosis and cystoid macular edema
Cellophane maculopathy
Optic atrophy
27. Indications for Enucleation
Absolute indications – Retinoblastoma and Malignant melanoma
Relative indications –
(i) Painful blind eye
(ii) Mutilating Ocular injuries
(iii) Anterior staphyloma
(iv) Phthisis bulbi
Eye donation from cadaver – most common indication
28. Organisms invading normal Corneal epithelium
Neisseria gonorrhoeae, Neisseria menigitidis
Cornyebacterium diphtheria
29. EOM supplied by 3rd Nerve
Superior Rectus
Inferior Rectus
Medial Rectus
Inferior Oblique
30. Two Causes of Complicated cataract
Inflammatory conditions – iridocyclitis, hypopyon Corneal ulcer
Degenerative conditions – Retinitis Pigmentosa, Retinal Dystrophies
Retinal detachment
Glaucoma, Intraocular Tumors – Retinoblastoma, Melanoma
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31. Two uses of Electroretinography
Diagnosis and prognosis of Retinal disorders such as RP, Retinal ischemia
To assess Retinal function when Fundus examination is not possible (in Dense cataract)
To assess Retinal function of babies where possibilities of impaired vision is considered
32. Two Anti mitotic drugs
5 fluorouracil
Mitomycin C
Indications – intermediate uveitis, peripheral ulcerative keratitis, OSSN
33. Two dyes used for Corneal staining :
Fluorescein
rose bengal
Alcian blue
34. Two types of tonometry :
Indentation tonometry – Schiotz tonometer
Applanation tonometry –
(I) Goldmann tonometer
(II) Perkin’s tonometer
(III) Pneumatic tonometer
(IV) Pulse air tonometer
(V) Tono pen
35. Two indications for Evisceration
Panophthalmitis
Expulsive Choroidal Hemorrhage
Bleeding Anterior staphyloma
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36. Anti VEGF Agents
Indications –
(i) Choroidal Neo vascularization (wet ARMD)
(ii) Retinal Neo vascularization
(Diabetic Retinopathy, Sickle cell Retinopathy, Neo vascular Glaucoma)
Drugs –
(i) Ranibizumab
(ii) Pegaptanib
(iii) Bevacizumab
37. Hyper mature cataract
When the mature cataract is left insitu, hyper maturity sets in.
Two types : Morgagnian and Sclerotic
Morgagnian cataract :
(i) Whole cortex liquefies and lens converted to bag of milky fluid
(ii) Small brownish nucleus settle at bottom
Sclerotic cataract :
(i) Cortex disintegrated and lens shrunken due to leakage of water
(ii) Anterior chamber become deep and iridodonesis is seen
38. Applanation tonometry
Introduced by Goldmann in 1954
Based on Imbert Fick Law ie., Pressure (P) = Force (W) / Area (A)
Commonly used Applanation tonometers are :
Goldmann tonometer
Perkin’s tonometer
Pneumatic tonometer
Pulse air tonometer
Tono pen
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39. Nyctalopia :
Also called Night blindness
Conditions where functioning of rods is deranged lead to Nyctalopia
Causes :
Vitamin A Deficiency
Tapetoretinal degeneration
Congenital high myopia
Familial congenital night blindness
Oguchi’s disease
40. Posterior synechiae
Adhesions between posterior Surface of iris and Anterior capsule of crystalline lens
Morphological types – Segmental, annular, total
Segmental – Adhesions of iris to lens at some points
Annular –
(i) 360 degrees adhesions of pupillary margin to Anterior capsule of lens.
(ii) Leads to formation of seclusio pupillae and iris bombe
Total –
(i) Plastering of total posterior Surface of iris to Anterior capsule of lens
(ii) Results in deep Anterior chamber
41. Clinical Features of Complicated cataract
Starts as posterior sub capsular Cortical cataract
Bread crumb appearance in Slit lamp examination
Polychromatic lustre of reds, greens, and blues are seen
Diffuse yellow haze seen in adjoining cortex
Lens become opaque giving chalky white appearance
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42. Preservation of donor cornea
Short term preservation up to 48 hours – preserved at 4 degree celsius
Intermediate storage up to 2 weeks – done in McCarey Kaufman & optisol medium
Long term storage up to 35 days – done by organ culture method or cryo preservation
43. Legal blindness
Vision in better eye <1/60 to perception of light
44. Causes of Vitreous Hemorrhage
Retinal tear, RD, PVD
Trauma to eye
Inflammatory diseases – acute chorioretinitis, periphlebitis retinae
Vascular Disorders – Hypertensive Retinopathy, CRVO
Metabolic disorders – Diabetic Retinopathy
Exudative age related macular degeneration
Blood dyscrasias – Retinopathy of Anaemia, Leukemia, polycythemia
Bleeding disorders – purpura, haemophilia, scurvy
Neoplasms – Acute necrosis in Retinoblastoma and Malignant melanoma of choroid
Others – Coat’s disease, radiation retinopathy, retinal capillary aneurysm
45. Differential diagnosis for Limbal nodule
TB conjunctiva
Phlycten
Ophthalmia nodosa
VKC
Cysticercus
Leprosy
Nevus
Dermoid
Lipodermoid
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46. Iris nodules
Typically seen in granulomatous uveitis
Koeppe’s nodules – situated in pupillary border and initiate posterior synechiae
Busacca’s nodules – situated near the collarette are large
47. Presbyopia
Physiological insufficiency of accommodation leading to a progressive fall in near vision
Condition of failing near vision due to age related decrease in the amplitude of accommodation
or increase in punctum proximum is called Presbyopia
Causes :
(i) Age related changes in lens – decrease in elasticity or Sclerosis of lens
(ii) Age related decline in ciliary muscle power
Symptoms :
(i) Difficulty in near vision
(ii) Asthenopic symptoms due to fatigue of ciliary muscle
Treatment :
(i) Appropriate convex glasses for near work
(ii) Presbyopic spectacles
(iii) Presbyopic bifocal LASIK
48. Three causes of preventable blindness
Vitamin A Deficiency
Trachoma
Refractive errors
49. Phlycten
Nodule occurring as an allergic response of conjunctival and Corneal epithelium to some
endogenous allergens
Causative allergens :
(I) Tuberculous Proteins
(II) Staphylococcal proteins
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(III) Proteins of Moraxella Axenfeld bacillus
Delayed hypersensitivity response to endogenous microbial proteins
Treatment :
(i) Topical steroids
(ii) Antibiotic drops
(iii) Atropine 1% eye ointment
50. Cycloplegics
Cause paralysis of accommodation and dilate the pupil
Commonly used Cycloplegics –
(i) Atropine 1% ointment
(ii) Homatropine 2% drops
(iii) Cyclopentolate 1% drops
Retinoscopy performed after instilling cycloplegics is called Wet Retinoscopy
51. Layers of Cornea
Epithelium
Bowman’s membrane
Stroma
Dua’s layer
Descemet’s membrane
Endothelium
52. Scleromalacia Perforans
Anterior necrotizing Scleritis without inflammation
Occurs in elderly females with long standing Rheumatoid Arthritis
Melting sclera together with overlying episclera and conjunctiva separates from normal sclera
due to obliteration of arterial supply
Spontaneous perforation extremely rare
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53. Types of Iridectomy
Iridectomy is an abscission of part of iris
Types –
(i) Peripheral iridectomy
(ii) Key – hole iridectomy
(iii) Broad or sector iridectomy
54. Causes of Childhood blindness
Vitamin A Deficiency
Measles
Conjunctivitis
Ophthalmia neonatorum
Congenital cataract
Retinopathy of Prematurity
55. Axial biometry
Axial biometry is the process of measuring the Axial length of the eyeball
Ocular A – scan is used for Axial biometry
It produces unidimensional image and echoes are plotted as spikes
Axial length of normal eye ball – 22.0 to 24.5 mm
56. Causes of cherry red spot
CRAO
Tay Sach’s disease
Niemann Pick’s disease
Gaucher’s disease
Berlin’s Oedema
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57. Evisceration and indications
Removal of the contents of eyeball leaving behind sclera
Indications –
(i) Panophthalmitis
(ii) Expulsive Choroidal Hemorrhage
(iii) Bleeding Anterior staphyloma
58. Social blindness and Legal blindness
Social blindness – Vision in better eye <3/60 to 1/60
Legal blindness – Vision in better eye <1 /60 to perception of light
59. Atropine
Commonly used Cycloplegic
Available as 1% Atropine sulphate eye drops or ointment
In iridocyclitis, Atropine
(i) Gives comfort and rest to eye by relieving spasm of iris sphincter and ciliary muscle
(ii) Prevents the formation of synechiae and break already formed synechiae
(iii) Reduces exudation, relives hyperaemia, reduce vascular permeability
(iv) Increases blood supply to Anterior uvea
60. Causes of Shallow Anterior chamber
Primary narrow angle glaucoma
Hypermetropia
Post operative shallow Anterior chamber
Malignant Glaucoma
Anterior perforations
Anterior subluxation of lens
Intumescent lens
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61. Causes of Symblepharon
Thermal or chemical burns
Membranous conjunctivitis
Injuries
Conjunctival ulcerations
Ocular Pemphigus
Steven’s Johnson syndrome
62. Define Ptosis
Abnormal drooping of upper eyelid is called Ptosis
Two types – Congenital and Acquired Ptosis
Causes of Acquired Ptosis :
Neurogenic Ptosis – 3rd Nerve palsy, Horner’s Syndrome, Multiple Sclerosis
Myogenic Ptosis – Myasthenia Gravis, Dystrophica Myotonica, Ocular Myopathy
Aponeurotic Ptosis – Senile Ptosis, Post operative Ptosis
Mechanical Ptosis – Lid Tumors, Multiple Chalazia
Treatment :
Congenital Ptosis – Fasanella Servat Operation, Levator resection, Frontalis sling surgery
Acquired Ptosis – Treat the cause
63. Common Fungi affecting cornea
Filamentous Fungi – Aspergillus and Fusarium
Yeasts – Candida
64. Two gram negative microorganisms
Escherichia coli
Klebsiella
Proteus
Pseudomonas
Neisseria gonorrhoeae
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65. Four signs of Thyroid Ophthalmopathy
Dalrymple’s sign – Retraction of upper eyelids producing staring look
Von Graefe’s sign – when globe is moved down upper eyelid lags behind
Enroth’s sign – Fullness of eyelids due to edema
Giffords sign – Difficulty in Eversion of upper eyelid
Stellwag’s sign – Infrequent blinking
66. Two common types of congenital cataract
Lamellar cataract
Blue dot cataract are the two most common types of congenital cataract
67. Advantages of indirect Ophthalmoscope
Ophthalmoscopy is a clinical examination of interior of eye by ophthalmoscope
Indirect Ophthalmoscopy is now very popular method for examining posterior segment
Advantages
(i) Visualisation through hazy media is possible due to inbuilt illumination.
(ii) Field of view is much larger than direct ophthalmoscopy
(iii) Examination of peripheral retina up to ora serrata is possible
(iv) Depth perception of the lesion is possible due to stereposis
(v) Visualisation of Fundus in very high refractive error is possible
68. Buphthalmos
Also called as Bull’s eye
Corneal enlargement seen in Congenital Glaucoma is termed as Buphthalmos
It occurs when the onset of congenital glaucoma is especially before 3 years
Normal Corneal diameter in infant is about 10.5 mm
Diameter more than 13 mm confirms Buphthalmos
Lacrimation, photophobia and blepharospasm - classical triad of congenital glaucoma
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69. Two eye drops to treat open angle glaucoma
Topical beta blockers – Timolol maleate 0.5% bd, Betaxolol 0.25% bd
Prostaglandin analogues – Latanoprost 0.005% HS, Travoprost 0.004% HS
Adrenergic drugs – Epinephrine hydrochloride, Brimonidine 0.2% bd
Dorzolamide – 2% bd
Pilocarpine – 2% tds
70. Causes of Aphakia
Congenital absence of lens
Surgical aphakia
Aphakia due to absorption of lens matter
Traumatic extrusion
Posterior dislocation
71. Treatment for chronic dacryocystitis
Conservative treatment by repeated lacrimal syringing
Balloon catheter dilatation
Dacryocystorhinostomy
Dacryocystectomy
Conjunctivo dacryocysto rhinostomy
72. Newer drugs in Glaucoma
Rho – kinase associated proteins inhibitor – Ripasudil
Adenosine receptor agonist
BkCa ionic channel modulator – Latanoprostene bunod
Latrunculinic derivatives
73. Four Causes of dislocated lens
Marfan’s syndrome Ehler’s Danlos syndrome
Homocystinuria Hyperlysinaemia, Sickler syndrome
Weil Marchesani Syndrome
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74. Vitamin A Prophylaxis
Infants 6 – 12 months and older child < 8kg - 1 lakh IU orally every 3 to 6 months
Children 1 to 6 years. - 2 lakh IU orally every 6 months
Lactating mothers - 20000 IU orally once at delivery
Infants < 6 months not breast fed. - 50000 IU orally before 6 years
75. Causes for Tubular vision
Glaucoma
Retinitis Pigmentosa
Retinal detachment
Ocular migraine
76. Vossius ring
It occurs due to blunt Trauma – closed globe injury
It is a circular ring of brown pigment seen on anterior capsule
Occurs due to striking of contracted pupillary margin against crystalline lens
It is always smaller than size of pupil
77. Ocular Hypertension
When patient has an IOP constantly more than 21 mm Hg but no optic disc and visual field
changes
High risk factors :
(i) Significant diurnal variation in values of IOP
(ii) Water drinking provocative test positive
(iii) Associated splinter Hemorrhages near or over Optic disc
(iv) Retinal nerve fibre large defects
78. Hutchinson triad
Common form of presentation of congenital syphilis
Interstitial keratitis
Malformed teeth of Hutchinson teeth
8th Nerve deafness
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79. Histopathology of Retinoblastoma
Small round cells with large nuclei
Flexner Wintersteiner rosettes
Homer Wright rosettes
Pseudo rosettes
Fleurettes formation
Necrosis and calcification
80. Grades of binocular Vision
Grade I – Simultaneous macular perception
Grade II – Fusion
Grade III – Stereposis
81. Two Differences between Pterygium and Pseudo Pterygium
Pterygium Pseudo Pterygium
Etiology Degenerative process Inflammatory process
Age Usually in elder persons Occurs at any age
Site Situated in palpebral aperture Occurs at any site
Stages Progressive, regressive or Always stationary
stationary
Probe test Probe cannot be passed Probe can be passed under
underneath neck
82. Causes for congenital cataract
Idiopathic
Hereditary – Trisomy 21, Stickler syndrome, cerebro oculo facial syndrome
Familial – Cataracta pulverulenta
Maternal factors –
(I) Malnutrition (III) Thalidomide or steroid ingestion
(II) Rubella, Toxoplasmosis, CMV (IV) Radiation exposure
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Fetal factors –
(I) Fetal anoxia (III) Congenital anomalies – Lowe
(II) Metabolic – Galactosemia, syndrome, Myotonia Dystrophica
Galactokinase deficiency (IV) Persistent Hyperplastic Primary
Vitreous
83. Siderosis and Chalcosis
Siderosis – Degenerative changes produced by an iron foreign body
Clinical manifestations
(i) Rusty deposits arranged radially in Anterior epithelium
(ii) Lens become cataractous
(iii) Iris first stained greenish then reddish brown
(iv) Pigmentary degeneration occurs in retina
(v) Secondary open angle type of glaucoma
Chalcosis – Specific changes produced by the alloy of copper in eye
Clinical manifestations
(i) Kayser Fleischer Rings occur in Descemet’s membrane of cornea
(ii) Sunflower cataract
(iii) Golden plaques in posterior pole of retina
84. Entropion and its types
Inturning of the lid margin is termed as Entropion
Types :
(i) Congenital Entropion
(ii) Cicatricial Entropion
(iii) Senile Entropion
(iv) Mechanical Entropion
Symptoms :
(i) Foreign body sensation (iii) Lacrimation
(ii) Irritation (iv) Photophobia
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85. Two Causes for sudden painless loss of vision
Central Retinal Artery Occlusion
Massive Vitreous Hemorrhage
Retinal detachment involving macular area
Ischemic Central Retinal Venous Occlusion
86. Accommodation – changes occurring in eye
Convergence of eye ball
Constriction of pupil
Increase in Anterior curvature of lens
87. Berlin’s Oedema
Also called Commotio Retinae
Common occurrence following a blow on the eye
Milky white cloudiness involving considerable area on posterior pole
Associated with cherry red spot in foveal region
Disappear after few days or replaced by pigmentary changes
88. Causes of Bilateral Proptosis
Developmental anomalies of skull – craniofacial dystosis
Osteopathies – Osteitis deformans, rickets, acromegaly
Inflammatory conditions – Mikulicz’s syndrome, Cavernous sinus Thrombosis
Endocrinal – Thyroid Associated Ophthalmopathy
Tumors – Symmetrical Lymphomas, Secondaries from Retinoblastoma
Systemic disorders – Systemic amyloidosis, Wegener’s granulomatosis
89. WHO Classification of Trachoma
TF – Trachomatous Inflammation – Follicular
TI – Trachomatous Inflammation – Intense
TS – Trachomatous Scarring
TT – Trachomatous Trichiasis
CO – Corneal Opacity
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90. Intravitrial drugs used in Endophthalmitis
Vancomycin 1 mg in 0.1 ml plus Ceftazidime 2.25 mg in 0.1 ml
Vancomycin 1 mg in 0.1 ml plus Amikacin 0.4 mg in 0.1 ml
Dexamethasone 0.4 mg in 0.1 ml
91. Two Causes for Rubeosis Iridis
Retinal ischemic diseases – CRAO, CRVO, Retinal detachment, Diabetic Retinopathy
Tumors – Choroidal Melanoma, Retinoblastoma
Inflammatory conditions – Uveitis, Bechet’s disease
Sympathetic Ophthalmia
92. Four Mydriatics
Atropine, Homatropine
Phenylephrine
Tropicamide
Cyclopentolate
93. Two main advantages of Phacoemulsification
Topical anaesthesia may be sufficient
Post operative congestion is minimal after Phacoemulsification
Small incision than SICS (3.2 mm)
Less Corneal Complications
Visual rehabilitation is comparatively quicker
Less post operative astigmatism
94. WHO definition for Blindness
Visual acuity of less than 3/60 or its equivalent. (1972)
Inability to count fingers in day light at a distance of 3 meters (1979)
95. Two Causes for toxic optic neuropathies
Tobacco Methanol
Ethanol Quinine
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96. Elevators of upper eyelid and Nerve Supply
Levator palperbrae superioris – Oculo motor Nerve
Muller’s muscle – Sympathetic Supply
97. Fundus findings in Grade 4 Hypertensive Retinopathy
Grade I – mild generalised arteriolar attenuation
Grade II – marked generalised narrowing, Salus’ sign +
Grade III – Grade II changes plus
- Copper wiring of arterioles
- Banking of Veins Distal to AV crossings (Bonnet sign)
- Tapering of veins on either side of crossings (Gunn sign)
- Right angle deflection of veins (Salus’ sign)
Grade IV – Grade III changes plus silver wiring and papilledema
98. Components of SAFE strategy
For Prophylaxis against Trachoma infection and prevention of blindness
S : Surgery for Trichiasis and Entropion – Tertiary Prevention
A : Antibiotics – Secondary Prevention
F : Facial Hygiene – Primary Prevention
E : Environmental cleanliness – Primordial prevention
99. Parameters to calculate IOL power : SRK formula
P = A – 2.5 L – 0.9 K
P = Power of IOL
A = Constant which is specific for each lens type
L = Axial length of the eyeball in millimeter determined by A scan
K = Average Corneal curvature determined by Keratometry
100. Two Viscoelastic substances
Methyl cellulose Hypromellose
Sodium Hyaluronate Chondratin sulfate
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101. Two syndromes associated with retinitis pigmentosa
a)laurence moon biedl syndrome
b) cockayne's syndrome
c) refsum's syndrome
102. Two causes of Lagopthalmosis
a.Facial nerve palsy
b.Leprosy
c.Myxoedema
103. Two cause of congenital cataract
a.Birth trauma
b.Down syndrome
c.Rubella
d.Lowe's syndrome
104. Ocular manifestations of human deficiency syndrome(any 2)
Retinal microvasculopathy Herpes zoster ophthalmicus
Toxoplasmosis- chorioretinitis
105. Two dyes used in opthalmology
a.indian ink - for tattooing cornea
b.Tryphan blue - to stain anterior capsule of lens during cataract surgery
Candida endophthalmitis
Burkitts lymphoma of orbit.
CLARENZ’16 ophthalmology TVMC
106.Two ocular signs of thyroid ophthalmopathy
Lid signs - retraction of upper eye lid : staring frightened appearance (dalrymple sign)
1.Lid lag(Von graefe's sign)
2.Fullness of lid(Enroth sign)
3.Difficulty in Eversion of upper lid( Gifford's sign)
4.Infrequent blinking ( Stellwag's sign)
5.Increased pigmentation of lid(Jellinek’s sign)
6.Poor forehead wrinkling on looking up (Joffroy's sign)
Conjunctional signs- deep injection and chemosis)
Papillary signs- inequality of pupil dilation
Ocular mobility defect- Mobius sign, restrictive ocular myopathy
Exophthamos
Exposure keratitis
Optic neuropathy
107. Two clinical features of trachoma
trachoma - causes chronic keratoconjunctivitis
two features-
a.pannus formation ,
b.corneal opacity ,
c.trichiasis
108.Drugs causing cataract:
1. Corticosteroids
2. Phenothiazine
3. Strong mitotics
CLARENZ’16 ophthalmology TVMC
109.Difference between direct and indirect ophtholmoscopy
Direct Indirect
opthalmoscopy opthalmoscopy
Condensing lens: not required Required
Image virtual erect Real inverted
Magnification 15 times 2.5 times
110. Post operative complications of keratoplasty
early complications
flat anterior chamber,iris prolapse,infection,secondary glaucoma,epithelial defects,primary
graft failure
late complications
graft rejection,recurrence of disease, marked astigmatism and cystoid macular edema
CLARENZ’16 ENT TVMC
1. Signs of retracted tympanic membrane
Loss of lustre
Loss of cone of light
Foreshortening of handle of malleus
Prominent lateral process
Sickle shaped anterior and posterior malleolar folds
2. Haller cell
It’s a part of anterior group of ethmoid air cells
Situated in floor of orbit
More common on left side
3. Causes of unilateral tonsillar enlargement
Peritonsillar abscess
Tonsillolith
Foreign body in tonsil
4.Conditions causing trismus
Peritonsillar abscess
Ludwig angina
Lingual tonsil abscess
5. Uses of laser in ENT
Argon- hemangioma, telangiestasia treatment, to create hole in stapes footplate
KTP- micro laryngeal surgery, endoscopic sinus surgery
Nd YAG- debunk esophageal and trachea bronchial lesions
CO2- transverse cordotomy
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CLARENZ’16 ENT TVMC
6. Carharts notch
Seen in otosclerosis
Bone conduction curve shows maximum loss at 2000Hz
Disappears after successful stapedectomy
7. Functions of Eustachian tube
ventilation and regulation of middle ear pressure
clearance of middle ear secretions
Protection against nasopharyngeal sound pressure
8. Cottles line
Imaginary line extending from anterior nasal spine of maxilla to nasal spine of
frontal bone
Anterior to this line septoplasty is done and submucosal resection extends
posterior to this line
9. Immediate complications of tracheostomy
Haemorrhage
Apnea following opening of an obstructed tube
pneumothorax
Aspiration of food
Injury to esophagus, laryngeal nerve
10. Major complications of FESS
Orbital haemorrhage CSF leak
Loss of vision Meningitis and brain abscess
Diplopia Intracranial haemorrhage
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CLARENZ’16 ENT TVMC
Injury to ICA, NLD
11. Prevertebral shadow widening
Opposite to C2 - more than 7mm or more than width of body of C2
Opposite to C6 - more than 14mm in children and 22mm in adults
Causes:Retropharyngeal and retroesophageal abscess
12. Laryngomalacia
Excessive flaccidity of supraglottic larynx which is sucked in during inspiration
producing stridor and cyanosis
Subsides in prone position
On direct laryngoscopy: omega shaped epiglottis
Most common congenital laryngeal anomaly
Rx: conservative, tracheostomy, supraglottoplasty
13 . Medical treatment of meniers disease
reassurance and psychological support
Bed rest with elevated head end
IV fluids and electrolytes administration
Vestibular sedatives- dimenhydrinate, promethazine, prochlorperazine
Diazepam 5-10mg I’ve
Vasodilator- carbogen (5%co2 with 95% o2)
14. Causes and treatment of secondary hemorrhage
Seen between post op day 5 to 10
Due to sepsis and premature separation of membrane
Rx: conservative management, suction if needed
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CLARENZ’16 ENT TVMC
15. Premalignant lesions of larynx
Squamous papilloma
Chondroma
Hemangioma
Granular cell tumor
Glandular tumor- oncocytoma
16. Complications of cortical mastoidectomy
Facial nerve injury
Dislocation of incus
Injury to horizontal semicircular canal
Injury to sigmoid sinus
Injury to Dura of middle cranial fossa
17. Unpaired cartilages of larynx
Thyroid
Cricoid
Epiglottis
18. Indications for radical mastoidectomy
Invasive cholesteatoma Removal of gloms tumour
Approach to petrosal apex Carcinoma middle ear
Failure of previous attempts
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CLARENZ’16 ENT TVMC
19. Causes of left recurrent laryngeal nerve palsy
Accidental trauma
Thyroid disease/ surgery
Bronchogenic cancer
20. Boundaries of parapharyngeal space
Base - base of skull
Apex- hyoid bone
Medial- buccopharyngeal fascia covering the constrictors
Posterior- prevertebral fascia covering prevertebral muscles and transverse
process of cervical vertebra
Lateral- medial pterygoid muscle, mandible, deep surface of parotid.
21. Complications of tonsillectomy
Immediate Delayed
Primary and reactionary hemorrhage Secondary hemorrhage
Injury to tonsillar pillars, uvula, teeth Infection
Aspiration of blood Lung complications
Facial edema Scarring in soft palate and pillars
Surgical emphysema
Tonsillar remnants
Hypertrophied lingual tonsil
22. Maxillectomy - types and indications
Types:
Medial maxillectomy Supra structure maxillectomy
Infrastructure maxillectomy Subtotal and total maxillectomy
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CLARENZ’16 ENT TVMC
Granulomatous lesions of maxilla
Indications: Maxillary fibrous dysplasia
Oral cavity malignancy
SCC of maxilla
23. Cricothyrotomy/ laryngotomy/ mini tracheostomy
Opening the airway through cricothyroid membrane
Skin in this area is incised vertically and cricothyroid membrane cut with
transverse incision and the space kept open
Uses: Buys time to allow patient to be carried to OT
Elective procedure to clear bronchial secretions post thoracic surgery
24. Littles area
Situated in anterior inferior part of nasal septum just above vestibule
Arteries forming vascular plexus (Kiesselbach plexus):
Anterior ethmoidal A.
Septal br of superior labial A.
Septal br. Of sphenopalatine A.
Greater palatine A.
Usual site of epistaxis
25. Esophageal / hypopharyngeal diverticulum
Pulsion diverticulum of pharyngeal mucosa which herniated through killians
dehiscence
Due to spasm of cricopharyngeal sphincter
Features: dysphagia, regurgitation, cough and aspiration pneumonia
Rx: dohlmans procedure, laser
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CLARENZ’16 ENT TVMC
26 . Indications of cochlear implant
1. Bilateral severe to profound 3. No medical contraindications
SNHL for surgery
2. No benefit from hearing aids
27. Levels of neck lymph nodes
1A- Submental
1B- Submandibular
2A- Upper jugular anterior to 11th cranial nerve
2B- Upper jugular posterior to 11th cranial nerve
3- Midjugular
4- Lower jugular
5- Posterior triangle
6- Prelaryngeal, pre and paratracheal
7- upper mediastinal
28. Otosclerosis – diagnosis and medical management
Diagnosis:
Schwartz’s sign- reddish hue on promontory through tympanic membrane
Normal Eustachian tube function
Negative rinne test, lateralisation of Weber’s test to ear with greater conductive
loss
PTA- loss of air conduction for lower frequencies , Carharts notch
Medical management:
Sodium fluoride given to hasten the maturity of focus and to arrest cochlear loss
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CLARENZ’16 ENT TVMC
29. Surgery for facial palsy
Nerve decompression of vertical or tympanic or labyrinthine segment
Approach- post aural and middle fossa approach
30. Gradenigo syndrome
Ear discharge
Diplopia
Retro orbital pain
Occurs due to petrositis as a complication of otitis media
31. Parts of hypopharynx
Pyriform sinus/fossa
Postcricoid region
Posterior pharyngeal wall
32. Rhinitis sicca
Crust forming disease seen in patients who work in hot,dry, dusty conditions
Characterised by squamous metaplasia with atrophy of seromucinous glands
Rx: bland ointment with steroid and antibiotic, nasal douche
33. Laryngocele
Dilatation of laryngeal saccule
Extends between thyroid cartilage and ventricle
Bryce sign- gurgling sound on pressing
Rx- excision
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CLARENZ’16 ENT TVMC
34 . Signs of malignant otitis externa
Excruciating pain Facial paralysis
Granulation tissue Cranial nerve palsies
35. Rehabilitation methods after total laryngectomy
Esophageal speech
Electrolarynx
Transoral pneumatic device
Tracheoseophageal speech
Aphonic lip speech
36. Features of laryngeal TB
Symptoms:
Weakness of voice
Hoarseness
Severe radiating pain to ears
Dysphasia
Signs:
Vocal cord hyperaemia
Pseudo edema of epiglottis/ turban epiglottis
Granulation tissue in inter-arytenoid region
37. Dangerous area of face
Comprises the area bounded by nose, upper lip and corners of mouth
Any boil or infection in this area can spread to cavernous in us resulting in
cavernous sinus thrombosis due to retrograde venous drainage of these areas to
cavernous sinus
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CLARENZ’16 ENT TVMC
38. Secretory otitis media
Also known as serous/mucoid otitis media, glue ear
Insidious accumulation of non-purulent effusion in middle ear cleft occurring in
school going age group
Causes:
Malfunctioning of Eustachian tube
Allergy
Unresolved otitis media
Viral infections
Characterised by hearing loss, defective speech, mild earache, tympanic
membrane retraction
Rx: decongestant, antihistaminics, myringotomy, grommet insertion
39. Tullio phenomenon
Vertigo induced by loud sound
Seen in congenital syphilis when 3 functioning windows are present- oval window,
round window, extra window- fistula of semicircular canal or fenestration
operation.
40. Vasomotor rhinitis
also known as non-allergic, non-infective perennial rhinitis
Due to unstable autonomic nervous system and hyper reactive nasal mucosa
which responds to nonspecific stimuli
Features: paroxysmal sneezing, excess rhinorrhea, nasal obstruction
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CLARENZ’16 ENT TVMC
41. Killians dehiscence
potential gap between thyropharyngeus and cricopharyngeus
Also known as gateway of tears
Site of perforation during esophagoscopy, site for herniation of pharyngeal
mucosa.
42. Achalasia cardia
Condition due to absence of peristalsis in body of esophagus and high resting
pressure in lower esophagus
Dysphagia more to liquids
Ba swallow- bird beak appearance
Rx: modified Heller myotomy
43. Trautmanns triangle
Boundaries
Anterior- bony labyrinth
Posterior- sigmoid sinus
superior- dura or superior petrosal sinus
It is a landmark to approach mastoid air cells after cortical mastoidectomy
44. Travelling wave theory of Von bekesy
A sound wave depending on its frequency reaches maximum amplitude on a
particular place on the basilar membrane and stimulates that segment.
45. Sulcus vocalis
Voice disorder that cause perpetual weaknesss and voice hoarseness
Due to thinning of laminate of vocal cords
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CLARENZ’16 ENT TVMC
46. Sialolithiasis/ salivary calculi
Formed by deposition of calcium phosphate on the organic matrix of mucin or
cellular debris
More common in submandibular gland
Meal time syndrome- intermittent swelling of gland and pain due to obstruction to
outflow of saliva at meal time
80% stones are radio opaque
47. Ventilation tube/ grommet
Inserted on the tympanic membrane to provide continued aeration of middle ear
Usually inserted in antero inferior quadrant
Used in otitis media with effusion when other treatment methods fail
48. Indications for total laryngectomy
Laryngeal cancers with
T3/T4 lesion
Invasion of thyroid/ cricoid cartilage
Bilateral arytenoid involvement
49. Intra-temporal complications of CSOM
Acute mastoiditis
Petrositis
facial paralysis
Labyrinthitis
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CLARENZ’16 ENT TVMC
50. Causes of referred otalgia
Via 5th cranial nerve- caries tooth,ulcers of tongue,ill fitting dentures..
Via 9th cranial nerve- acute tonsillitis, peritonsillar abscess
Via 10th- ulcers of larynx, esophgagus
Via C2,C3- cervical spondylosis
51. Tonsillolith
Crypt of tonsil blocked with debris
Made of inorganic salts of calcium and magnesium
Rx: removal of stone/ tonsillectomy
52. Functional aphonia
Hysterical abduction of vocal cords on phonation in the presence of normal
adductors
more common in emotionally labile females of 15-30 yrs
Rx: reassurance, psychotherapy
53. Furuncle of nose
Acute infection of hair follicle of nasal vibrissae
By staphylococcus aureus
Exquisitively painful and tender lesion
Rx: warm compress, analgesics, antibiotics, I&D
Complications: cavernous sinus thrombosis, upper lip cellulitis, septal abscess
54. Clinical features in fungal sinusitis
Mucor- vasculoinvasive; causes ischemic necrosis with black eschar
Aspergillus- acute fulminant sinusitis with tissue invasion
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CLARENZ’16 ENT TVMC
55. Common sites of CSF leak in nose
Frontal sinus
Cribriform plate
Roof of ethmoid air cells
Sphenoid sinus
56. Functions of nose
Respiration Vocal resonance
Air conditioning of inspired Nasal reflex
air Olfaction
Protection of lower airway
57 . Laryngeal papillomatosis
Juvenile type- by HPV 6, 11
Most common benign laryngeal neoplasm in children
Adult type- single, smaller, arise from anterior half of vocal cord
Rx: micro-laryngoscopy, CO2 laser excision, IFN 2alpha, 13 CIS retinoic acid
58. Aphthous ulcers
Recurrent, superficial ulcers of oral cavity sparing hard palate and gingiva
Minor form- more common, ulcers are 2-10 mm size, multiple with central
necrosis & red halo
Major form- 2-4 cm size, heals with scar followed by another ulcer
59. Complications of septal surgery
Bleeding Perforation
Septal hematoma Depression of nasal bridge
Septal abscess Flapping of nasal septum
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CLARENZ’16 ENT TVMC
60. Surgical management of atrophic rhinitis
Young’s operation - bilateral occlusion of nostrils by flaps
Modified Young’s operation- partial closure
Narrowing of nasal cavities by Teflon, fat, cartilage..
61 . Investigations for dysphagia
Detailed history
Clinical examination
Blood investigation to know nutritional status and to rule out Plummer Vinson
syndrome
Chest X-ray
X-ray neck lateral view
Barium swallow to rule out achalasia,strictures, diverticula
Manometers to rule out esophageal motility disorders
Esophagoscopy
62. Quinsy
Peritonsillar abscess following acute tonsillitis
Causes: s.pyogenes, s.aureus, anaerobes
Presents with septicaemia, severe throat pain, hot potato voice, trismus
Rx: I&D, hospitalisation and i.v antibiotics, analgesics, oral hygiene
63. Otogenic brain abscess
Sequelae of csom in adults and acute otitis media in children
Direct extension of middle ear infection through tegmen or by retrograde
thrombophlebitis
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CLARENZ’16 ENT TVMC
4 stages:
Invasion/ initial encephalitis
Localization/latent abscess
Enlargement/ manifest abscess
Termination/.rupture of abscess
64. Bilateral abductor paralysis
Bilateral recurrent laryngeal nerve palsy occurring after thyroid surgery or
malignancy
Position of vocal cord: median/paramedian
Presents as dyspnea/stridor
Rx: tracheostomy, transverse cordotomy(kashima operation)
65. Pure tone audiometry
It is a measure of threshold of hearing by air and bone conduction and thus degree
and type of hearing loss
66. Masking
When difference in air conduction thresholds between two ears is 40dB or more
masking is done
It avoids getting a shadow curve from non-test better ear
Done by narrow band noise / barany box
67. Keratosis obturans
Collection of pearly white mass of desquamated epithelial cells in deep meatus
Due to its pressure effect it causes absorption of meatal bone exposing facial
nerve
Rx: syringing, keratolytics like 2%salicylic acid in alcohol
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CLARENZ’16 ENT TVMC
68. Bell’s palsy
Idiopathic peripheral facial paralysis of acute onset
Etiology:
Viral infection Hereditary
Vascular ischemia Autoimmune disorder
Features: bell’s phenomenon, epiphora, facial asymmetry, ear pain, noise intolerance
69. Rhinolith
Stone formation around the nucleus of small foreign body, blood clot or inspissated
secretions by slow deposition of ca and mg
Leads to pressure necrosis
Features: epistaxis, neuralgic pain
Rx: removal under GA, lateral rhinotomy
70. Sluders neuralgia
Neuralgic pain in lower half of face along with
Nasal congestion
Rhinorrhea
Increased lacrimation
It’s due to neralgia of sphenopalatine ganglion
71. Obstructive sleep apnea (OSA)
Apnea occurring during sleep due to collapse of upper airway—> CO2 retention—>
pulmonary constriction —> congestive heart failure, cardiac hypoxia, hypertension
Gold standard diagnosis: polysomnography
Rx: weight reduction, diet modification, cpap, upper airway surgery
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CLARENZ’16 ENT TVMC
72. Reactionary haemorrhage
Haemorrhage after tonsillectomy occurring within 24hrs
Due to the presence of a clot which prevents the clipping action of superior constrictors
Rx: clot removal, application of pressure/ vasoconstrictor, ligation and electro
coagulation of bleeding vessel
73. Dysphagia lusoria
Compression of esophagus by aberrant right subclavian A. causing dysphagia
Here, Rt. Subclavian A. Arises from thoracic aorta and passes in front of or behind the
esophagus
74. Adenoid facies
Elongated face with dull expression
Open mouth
Prominent and crowded upper teeth
Hitched up upper lip
Pinched in nose
High arched hard palate
75. Turban epiglottis
Due to infiltration of epiglottis caused by laryngeal TB.
76. Fistula test
In the presence of fistula between external auditory canal and labyrinth, pressure
changes in external canal can be transmitted to labyrinth producing nystagmus.
Done by applying intermittent pressure to Targums or by siegels speculum
Positive in cholesteatoma, fenestration operation, post stapedectomy fistula,
round window membrane rupture
False positive in congenital syphilis, meniere disease (hennebert sign)
False negative in cholesteatoma covering the fistula site
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CLARENZ’16 ENT TVMC
77. Rhinoscleroma
Caused by gram negative coccobacillus Klebsiella rhinoscleromatis
3 stages- catarrrhal, granulomatous and cicatrising
Causes woody infiltration of upper lip
Histology: Mickulicz cells and Russell bodies
78. Waldeyers ring
Aggregation of subepithelial lymphoid tissue masses scattered throughout
pharynx
Adenoids
Palatine tonsil
Lingual tonsil
Tubal tonsil
Lateral pharyngeal bands
Nodules in posterior pharyngeal wall
79. Greisingers sign
Edema over mastoid seen in lateral sinus thrombosis
Due to thrombosis of mastoid emissary vein impending the venous drainage
80. Blood supply of tonsil
Tonsillar branch of facial a.
Ascending pharyngeal a. From external carotid
Ascending palatine branch of facial a.
Dorsal lingual branches of lingual a.
Descending palatine branch of maxillary a.
81. Potato nose/ rhinophyma
Hypertrophy of sebaceous glands of nose
Associated with acne rosacea
Rx: CO2 laser excision
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CLARENZ’16 ENT TVMC
82. Reinkes space
Potential sub-epithelial space in vocal cords
Boundaries:
Above and below :Arcuate line
In front : Anterior commissure
Behind: vocal process of arytenoid
83. Steeple sign
Seen in acute laryngotracheobronchitis
On AP view of neck X-ray
84. Impedance audiometry
Objective test for hearing
It consists of tympanometry and acoustic reflex measurements
85. Sermons law
“In a progressive lesion of recurrent laryngeal nerve, the abductors are paralysed first
before the adductors”
86. Wagner grossman theory
In complete paralysis of recurrent laryngeal nerve the cord lies in the paramedian
position because the ntact cricothyroid muscle adducts the cord.
87. Woodruffs plexus
Plexus of veins situated inferior to posterior end of inferior turbinate
Site of posterior epistaxis in adults
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CLARENZ’16 ENT TVMC
88. Trotters triad
Seen in nasopharyngeal carcinoma which spreads laterally to involve sinus of morgagni
involving mandibular nerve
Components
Conductive hearing loss
Ipsilateral immobility of soft palate
Neuralgic pain along V3
89. Samter triad
Nasal polyps
Bronchial asthma
Aspirin insensitivity
90. Hidden areas of larynx
Infrahyoid epiglottis
Anterior commissure
Subglottis
Ventricle
Apex of pyriform fossa
91. Freys syndrome/ gustatory sweating
Complication of parotid surgery
Sweating and flushing of preauricular skin during mastication
Result of aberrant innervation of sweat glands by parasympathetic secretomotor fibres
Rx: tympanic neurectomy, subcutaneous botulinum toxin, rising flap
92. Middle ear risk index (MERI)
To predict success of middle ear reconstruction procedures
Based on several factors like otorrhea, presence of granulation tissue, perforation.
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CLARENZ’16 ENT TVMC
93. Paterson brown Kelly / Plummer Vinson syndrome
Includes
Iron deficiency anemia
Esophageal web
Angular ceilings and koilonychia
Risk factor for post cricoid carcinoma
94. Rhinomanometry
Measures pressure changes in nasal cavity
Objective test
To calculate nasal resistance
95. Tolosa hunt syndrome
Unilateral orbital pain with episodic palsies of cranial nerves 3,4,6.
There is granulation tissue in cavernous sinus, superior orbital fissure or orbit
Rx: steroids
96. Eagle syndrome
Occurs due to elongated styloid process impinging on glossopharyngeal nerve
Features: discomfort in throat, ear pain, dysphagia, pain in upper neck
97. Battle sign
Ecchymosis over mastoid
Seen in temporal bone fractures
98. Paracusis willisii
Otosclerotic patient hears better in noisy than in quiet surroundings. This is because a
normal person will raise his voice in noisy surroundings
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CLARENZ’16 ENT TVMC
99. Complications of stapedectomy
Tear of tympanomeatal flap
Injury to chorda tympani
Incus dislocation
Vertigo
Conductive loss
100. Reinkes edema
Collection of fluid in reinkes space
Due to vocal abuse and smoking
Rx: longitudinal incision and drainage of gelatinous fluid
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CLARENZ’16 ENT TVMC
101.Acute Epiglotitis -organism and radiological findings:
• It is an acute inflammatory condition confined to the supraglottic structures
i.e. Epiglottis ,aryepiglottic folds and arytenoids
• Aetiology
H.influenza B
• Radiological findings
Thumb sign – lateral soft tissue x-ray of neck may show swollen epiglottis
102.Cricothyroid membrane -Surgical importance
• Cricothyrotomy/laryngotomy/mini tracheostomy
• A transverse incision is made in the cricothyroid membrane
• This space is kept open with a small tracheostomy tube
• Its used as
Elective procedure – to clear bronchial secretions following thoracic surgery.
Emergency procedure- till patient can be intubated or Tracheostomized.
103.Two causes of objective tinnitus:
1) vascular
• AV shunts
Congenital AV malformations
Glomus tumour of middle ear
• Arterial bruit
Carotid aneurysm
Carotid atenosis
• Venus hum
Dehiscent jugular bulb
2) Patulous eustachian tube.
3) Palatal myoclonus.
4) Tensor tympani myoclonus.
5) clicking of TM joint.
CLARENZ’16 ENT TVMC
104. Saddle nose deformity:
• Depression of nasal dorsum involving
Bony (or)
cartilaginous (or)
Both Bony and cartilaginous components of the nasal dorsum
• Aetiology:
Nasal trauma
As a complication of SMR
Destruction of septal cartilage by
a. Hematoma or abscess
b. Leprosy
c. Tuberculosis
d. Syphilis
• Treatment:
Augmentation rhinoplasty.
105. water's view:
• occipitomental view (or) nose-chin position. It is taken in such a way of that the nose and chin of
the patient touch the flim while the x ray beam is projected from behind
structures seen:
• maxillary sinus
• frontal sinus
• sphenoid sinus( if the flim is taken with open mouth)
• zygoma
• zygomatic arch
• nasal bone
• frontal process of maxilla
• superior orbital fissure
• intra temporal fossa
CLARENZ’16 ENT TVMC
106. Ramsay hunt syndrome
• Also known as Herpes zoster oticus There is facial paralysis along with vesicular rash in the
external auditory canal and pinna.
• There may also be anaesthesia of face,giddiness and hearing impairment due to involvement of
5th and 8th nerves.
107. Singer's nodule:
• Also called vocal nodules or Screamer's node.
• They appear symmetrically on the free edge of vocal cord, at the junction of anterior
1/3rd with the posterior 2/3rd.
• This is the area of maximum vibration of the cord and thus subject to maximum trauma
• It is caused by vocal trauma or vocal abuse
• It causes oedema and haemorhage in the submucosal space which undergoes
hyalinization and fibrosis.
• The overlying epithelium also undergoes hyperplasia forming a nodule
• Early stage-Soft, reddish, oedematous
• Later stage - Greyish colour or white in colour.
108. Retrocolumellar vein.
• It runs vertically downwards just behind the columella, crosses the floor of nose. and
joins venous plexus on the lateral nasal wall.
• This is the common site of venous bleeding in young people.
109. Intratympanic Gentamycin.
• Also called chemical labyrinthectomy.
• It is vestibulotoxic.
• on daily or bi-weekly injections into the middle ear it is absorbed through the round window and
causes destruction of the vestibular Labyrinth, thus controlling vertigo.
• Hearing loss has been reported in some cases.
CLARENZ’16 ENT TVMC
110. pleomorphic adenoma.
• It is a benign tumour of salivary glands.
• It is a slow growing tumour.
• They are called mixed tumours because both epithelium and mesenchymal elements are seen in
histology.
• Though it is encapsulated, it sends pseudopods into the surrounding gland which are left behind
if tumour is simply shelled out.
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