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Pediatric Joint Pain Insights

The document provides an overview of the approach to evaluating joint pain in pediatrics, including discussing the etiology, history, examination findings, and investigations for conditions that can cause arthralgia or arthritis. It describes how to differentiate between arthralgia and arthritis based on physical exam findings and lists common causes of joint pain categorized by etiology such as infection, trauma, rheumatic diseases, and hematological disorders. The document outlines the key aspects of history to obtain and physical exam findings to look for in order to determine the underlying cause of a patient's joint pain.

Uploaded by

Shivangi Lodha
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPTX, PDF, TXT or read online on Scribd

Topics covered

  • Acute Conditions,
  • Cultural Considerations,
  • Reassurance Techniques,
  • Hematological Disorders,
  • Etiology,
  • Rheumatic Diseases,
  • Laboratory Tests,
  • Systemic Symptoms,
  • Trauma,
  • Epidemiology of Joint Pain
0% found this document useful (0 votes)
205 views49 pages

Pediatric Joint Pain Insights

The document provides an overview of the approach to evaluating joint pain in pediatrics, including discussing the etiology, history, examination findings, and investigations for conditions that can cause arthralgia or arthritis. It describes how to differentiate between arthralgia and arthritis based on physical exam findings and lists common causes of joint pain categorized by etiology such as infection, trauma, rheumatic diseases, and hematological disorders. The document outlines the key aspects of history to obtain and physical exam findings to look for in order to determine the underlying cause of a patient's joint pain.

Uploaded by

Shivangi Lodha
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPTX, PDF, TXT or read online on Scribd

Topics covered

  • Acute Conditions,
  • Cultural Considerations,
  • Reassurance Techniques,
  • Hematological Disorders,
  • Etiology,
  • Rheumatic Diseases,
  • Laboratory Tests,
  • Systemic Symptoms,
  • Trauma,
  • Epidemiology of Joint Pain

Approach to Joint

Pain

Presenter – Dr Sourabh Soni


Junior Resident
Dept of Paediatrics
Moderator – Dr Gunjan Kela
Professor and HOD
Dept of Paediatrics
Overview
• Introduction
• Etiology
• History
• Growing pain
• Examination
• pGALS
• Investigation
Introduction
Arthralgia and Arthritis

Arthralgia : Joint Pain

Arthritis : Intrarticular swelling


Or
Two or more of the following signs:
1. Limitation in the range of motion
2. Tenderness or pain on motion
3. Warmth
4. Erythema
Etiology
Arthralgia Arthritis
• Infection: Rheumatic fever,Dengue • Rheumatic causes : Systemic lupus erythematosus(SLE)
• Trauma Juvenile dermatomyositis(JDM)
• Malignancy Vasculitis, Behcets disease ,Sarcoidosis,
• Rheumatic : Juvenile idiopathic arthritis Kawasaki disease, Henoch Schonlein
• SLE,Juvenile Dermatomyositis purpura(HSP)
• Scleroderma • Non Rheumatic causes:
• Hematological : Sickle cell disease 1> Malignancy
• Vascultitis : HSP,Kawasaki disease 2> Infective- Viral – Chikungunya, Rubella, Hepatits-B,
PAN,Wegener’s granulomatosis Parvovirus B, Ebstein Bar Virus(EBV)
Sarcidosis Bacterial- Osteomyelitis
• Reactive arthritis Tubercular
• Benign syndromes : Ehler danlos syndrome Lyme disease
• Pain syndromes : Fibromyalgia 4> Post-infectious : Acute rheumatic fever
• Nutritional : Rickets,Scurvy,Anaemia Reactive arthritis
• Psychogenic • Trauma
Number of Joints involved
What to ask?
• Age
• Sex
• Mode of onset and duration of joint involvement
• Single or Multiple joint
• Small or Large joint
• Axial or Appendicular
• Nature of pain :Migratory or additive
• Restriction of movement/Local erythema/Warmth
• H/o Trauma, illness or drug intake
• H/o Fever or other systemic manifestations
• Relationship of Pain to Activity
• H/o Bleeding diathesis
• Is the child suffering from any Blood disease
• Dietary history
• Polyarticular JIA
Age
• Kawasaki disease Early Childhood (2 - 5 years)
• HSP

• Psoriatic arthritis
• Juvenile Dermatomyositis Mid Childhood ( 6-11 years)
• Polyarteritis Nodosa

• Enthesitis Related Arthritis(ERA) Late childhood or


• Systemic Lupus Erythematosis(SLE) Early adolescence (12- 18 years)
Sex
• SLE Girls
• JIA

• Kawasaki disease
• Polyarteritis nodosa Boys
• Inflammatory bowel disease
• Enthesitis related arthritis

• Systemic onset Juvenile Idiopathic Arthritis = Equal distribution


Mode of onset and duration
Duration Examples
Acute : < 2 weeks Septic Arthritis,Trauma,Acute rheumatic fever,HSP

Subacute : 2 to 6 weeks Systemic lupus erythematosus,Reactive arthritis,


Polyarteritis Nodosa,Dermatomyositis,Leukemia
Sickle cell disease, hemarthrosis

Chronic : > 6 weeks Juvenile Idopathic Arthritis ,Tubercular, Psoriatic arthritis


Enthesitis related Arthritis(ERA)
History of preceeding events
Sore-throat or Scarlet fever – Acute Rheumatic Fever
GI symptoms- Reactive arthritis,Inflammatory bowel disease
GI infections – Salmonella
Urethritis –Reiter’s disease
Viral infections- Rubella,Mumps,chickenpox,Infectious mononucleosis,Hepatitis B
Recent immunization: Rubella
Trauma: Septic arthritis,Hemarthrosis,Effusion,strained ligaments,sprained muscles,
dislocation, fractures

Pyoderma : Septic arthritis


H/o drugs : Penicillin,Immunoglobulin, Antitoxin
H/o Koch contact
Site
• Distal interphalangeal joint : Psoriatic arthritis

• B/L Temporomandibular joint : RA factor Negative Polyarthritis

• Knee/Ankle joints : Reactive arthritis


Fever
• High grade fever with chills with joint swelling- Septic arthritis

• Long standing,low grade and continuous fever- Tuberculosis

• Prolonged high grade and irregular fever with remissions:


Idiopathic arthritis and SLE

• Prolonged fever with joint involvement : Leukemias


Deforming/Non- Deforming
Long standing/Aggressive disease :
Causes- Malalignment of articular structure
Soft tissue contracture
Fibrosis/Ankylosis

e.g.- RA factor +ve Polyarticular JIA


Pain
• Onset : Acute and related to specific trauma is commonly related to
Fractures
• Pain that worsens on activity: Destructive joint pain
• Pain with morning stiffness that improves on activity : JIA
• Pain that worsens on massage : Inflammatory joint pain
• Pain that improves on massage : Growing pains ( Usually occurs at
night and disappear in the morning
• Night pain : 1.) Malignancy( Osteiod osteoma)-Refractory or Unremitting pain
Persistant night waking
2.) Growing pains
• Pain in infectious cause has no diurnal variation
• Fleeting pain(Migratory): Acute Rheumatic Fever
Growing pains
• Benign nocturnal pains of childhood
• Peak age : 4-12 years
• M/C cause or reccurent musculoskeletal pain in children
• Intermittent and Bilateral
• Involves : Anterior Thigh, Shins and calf but not the joint
• In late afternoon or evening,wake the child from sleep
• Resolves quickly on massage/analgesics
• Disappear in the morning
• Treatment : Reassurance,Education,Massage during the episode, Muscle
stretching, NSAIDs may be used in frequent episodes
H/o Bleeding

• Bleeding from Gums : Scurvy


• Bleeding in joint on trivial injury : Hemophilia
• Bleeding P/R : HSP

H/o Hematological diseases :


• Sickle cell disease
• Leukemia
• Hemarthrosis in Hemophilia

Cardiac Symptoms:
• Exertional dypnea
• Palpitation
• Chest pain
Examination
• Local examination of joints
• Examination of spine
• Examination of muscles
• Presence of rash/subcutaneous nodules
• Lymphadenopathy/sinuses
• Eyes
• Oral cavity
• Desquamation of fingers
• Focus of infection
• Organomegaly
• Cardiovascular system
• Nails and Hair- Alopecia, Nail pitting,Onycholysis
• Gangrene and Stroke : SLE, Antiphospholipid Antibody syndrome(APLA)
• Renal system : Nephritis, nephrotic syndrome, hypertension in
JIA,SLE,PAN,KD,HSP
Inspection
• General body habitus including signs of cachexia, Pallor and Nutritional
deficiencies
• Balance,posture and gait pattern
• Skin-Rashes, Café-au-late spots,Hairy patches,Dimples,Cyst,Tuft of hair
or evidence of Spinal midline defects
• Spinal asymmetry,axial or appendicular deformities and evidence of
muscle spasm or contractures
• Muscle atrophy
• Range of motion of all joints,their stability and any evidence of
hyperlaxity
Palpation
• Local temperature
• Tenderness
• Swelling or mass
• Spasticity
• Contracture
• Bone or joint deformity
• Limb length
Examination of Joints
• Swelling,pain,tenderness and range of movements
• Arthralgia/Arthritis
• Single / Multiple
• Large joint affected in lower extremities i.e. Knee/Ankle : Oligoarticular JIA
• Small joints of upper or lower extremities : Polyarticular JIA
• Spindle shaped fingers : Rheumatoid arthritis
• Diffuse swelling of entire dorsum of hand and foot : Sickle cell disease
• Scorbutic beading of costochondral joint : Scury
• In TB hip joint : Limb is flexed,abducted and medially rotated
• Pseudoparalysis(Inability to move joint due to severe pain) : Septic
arthritis
• Examination of spine for kyphosis/scoliosis: TB spine

• Examination of muscles:
• Wasting above or below a joint is seen in idiopathic
arthritis or chronic involvement(Disuse atrophy)
• Tenderness of muscles : Dermatomyositis
Skin
• Erythema marginatum : Acute Rheumatic fever

• Salmon colored ( faint evanescent macular rash) : Systemic onset Juvenile


idiopathic arthritis(SJIA)
• Malar rash (butterfly shaped,sparing nasolabial fold) : SLE
• Palpable purpuric rash( extensor aspect-extremities) : HSP
• Heliotrope rash over upper eyelids and Gottron’s papules :
Dermatomyosistis
• Purpuric and ecchymotic patches :Leukemia

24
• Erythematous rashes with silvery white scales :
Psoriatic arthritis

• Subcutaneous nodules(extensor aspect of upper


extremities and suboccipital region) : Rheumatic fever
Eyes
• Pallor and Jaundice with symmetrical painful swelling of hand and
feet : Hand foot syndrome (Sickle cell disease)

• Uveitis: JIA

• Conjuctival redness : Kawasaki disease


Oral cavity
• Gum bleeding / spongy gums : Scurvy

• Swollen tongue(strawberry tongue and cracked lips)


- Kawasaki disease
- SLE
Organomegaly
• Hepatosplenomegaly : Collagen diseases
Leukemias
Disseminated TB

Splenomegaly : Sickle cell disease

Focus of infection : Boils


Abscess
E.g.- Septic Arthritis
CVS
• Hypertension : SLE
• Pericardial rub/Pericarditis: Rheumatoid arthritis
SLE
• Myocarditis : Rheumatoid arthritis and Kawasaki disease
pGALS
paediatric Gait,Arms,Legs and Spine

• Developed to detect inflammatory joint disease but can also detect


other Musculoskeletal disorders.

• Screening test for the assessment of school aged children based on


the adult GALS screen

• Consist of basic clinical maneuvers


Screening questions
• Ask for pain/stiffness in joint,muscle or back

• Ask for difficulty in getting dressed without any help

• Ask for difficulty in going up and downstairs


Gait
• Observing the child walking
• Asking the child to walk on tip-toes and heels

Arms
• Moving hands in different directions
• Making a fist
• Touching fingertips with thumb
• Squeezing metatarso-phalangeal joints
Legs
• Bending and straightening knees
• Passive flexion and extension of hip
• Feel for knee effusion

Spine :
Lateral flexion of cervical spine, bending forwards to
touch toes, observe spine from side and behind.
Investigations
• CBC
• ESR,CRP
• Coagulation factor
• Rheumatoid factor(RA)
• Liver function test
• Renal function test
• Antibodies – ANA,Anti-DNA
• ASO titre
• Culture-Throat swab,joint fluid,stool,urine
• Mantoux test
• Slit lamp examination of eyes
• Radiological investigations : Xray,USG,MRI
CBC
• Anemia – Sickle cell disease
Leukemia
• Leukocytosis(Polymorphonuclear predominance) – Septic arthritis
• Leucopenia with lymphopenia – SLE
• Reticulocytosis- Sickle cell disease
• Thrombocytopenia- Leukemia
• Thrombocytosis – Idiopathic arthritis
• Anemia of chronic disease- Collagen vascular disease,TB
• ESR – increased in Collagen diseases and Rheumatic fever.
• Clotting factors- Hemophilia
• Mantoux test – Tubercular
• Xray – Scurvy, TB, Idiopathic arthritis
• RA factor- Polyarticular JIA
• ANA seropositivity – increased in chronic uveitis in JIA
• Anti dsDNA – Highly specific for SLE
• ASO titre and Throat swab culture- Recent Streptococcal infection(Rising
titre-Rheumatic arthritis)
• CRP-Acute Rheumatic arthritis
• Urinalysis- Albumin and hematuria
• Synovial fluid aspiration – Microscopy and culture in Septic arthritis
• USG and MRI – Septic and tubercular arthritis and Hemarthrosis
• CRP-Acute Rheumatic arthritis
• Urinalysis- Albumin and hematuria
• Synovial fluid aspiration – Microscopy and culture in Septic arthritis
• USG and MRI – Septic and tubercular arthritis and Hemarthrosis
Case scenario

Case 1

A 6 year-old boy was brought with lower limb pain which happened
at [Link] was relieved with oil massage and paracetamol. Next day
morning the child woke up as if nothing happened over [Link]
following week he has a similar episode. This causes significant
anxiety in the family, and they immediately visit the primary
physician.
Diagnosis

Growing Pain
Case 2
• A 12-year-old boy was admitted to Hospital for multiple sites of arthralgia. He had
presented at the local clinic after experiencing fever, diarrhea, and abdominal
pain for 5 days, for which he had received successful [Link] week after
the onset of the enteritis, he developed generalized limb pain followed by large
joint involvement i.e. bilateral sacroiliac, wrist, and ankle [Link] had never
received a blood transfusion and had no history of sexual contact.
On admission-
Conscious
Temp -38℃(Febrile)
Pulse-115 beats/min
Blood pressure -110/70 mmHg
Physical examination-:
Swelling and tenderness of left ankle joint
Tenderness on motion
Pain over the bilateral wrist and left sacroiliac joints
Systemic examinations- Normal

A- Swelling of left ankle joint


B- Normal right ankle joint
• Laboratory studies showed
Hemoglobin-12.8 g/dL
WBC- 21,860/mm3
Platelets- 573,000/mm3,
ESR -74 mm/hr
CRP- 3.97 (0 to 0.5) mg/dL
Liver and renal function tests – Normal
VDRL – Negative
ANA – Negative
Urinalysis - Pyuria, but
Urine culture – Negative
HLA class I serotyping - Positive for B27
Synovial fluid(left ankle and left hip joint)- Severe inflammation but
Gram staining and Culture of this synovial fluid - Negative
Stool culture – Positive for Salmonella group D

Radiographs of the ankle joint - Soft tissue swelling, without erosive joint
damage
Diagnosis

Enthesitis related Arthritis


Thank You

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