Rheumatology Flashcards

1
Q

What is Juvenile Idiopathic Arthritis?

A

Inflammation of one or more of your joints that occurs before you turn 16.

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2
Q

What are the key features of JIA?

A
Arthritis for at least 6 weeks
Morning stiffness or gelling
Irritability of refusal to walk in toddlers
School absence or limited ability to participate in physical activity. 
Rash/fever
Fatigue
Poor appetite/weight loss
Delayed puberty
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3
Q

What are the signs of JIA?

A
Swelling in periarticular soft tissue oedema
Intraarticular effusion
Hypertrophy of synovial membrane
Swollen tendons
Pain
Joint held in position of max comfort
Limited ROM at extremes
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4
Q

How does Oligoarthritic JIA present?

A

Early onset more common
Girls 1-5
4 or less joints with no symmetry.
If early onset then 20-30% develop uvititis and test positive for ANA.
If late onset then test negative for ANA and no extrarticular manifestation.

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5
Q

How does pauciarticular JIA present?

A
Late onset more common
Boys over 8yrs
4 or fewer joints, no symmetry. 
Knees, ankles and hands
No hip involvement
Hip involved in late stage
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6
Q

How does Polyarticular JIA present?

A

5 or more joints
Few or no systemic manifestations of disease
Seropositive more common in >8yrs.
Seronegative more common in <5yrs.
large fats growing joints mostly affected
Systemic manifestations rare.
Mostly insidious onset.

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7
Q

What classifies enthesitis-related JIA?

A
Need at least 2 of following:
Onset of poly arthritis/oligoarthritis in boy > 8. 
HLA-B27 positive
Acute anterior uveitis
Family Hx of enthesitis related JIA
Sacroiliac joint tenderness
Inflammatory spinal pain.
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8
Q

What classifies Psoriatic JIA?

A
All are HLA-B27 positive
Need 2 of following 3:
Dactylitis
Family hx of psoriasis
Onycholysis (nail pitting)
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9
Q

What are some systemic features of JIA?

A
Intermittent fever > 2weeks
Salmon pink erythematous rash
Generalised lymphadenopathy
Serositis
Hepato/splenomegaly
High inflammatory markers
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10
Q

What are some investigations for JIA?

A
Examination
Plain x-ray
US
MRI with contrast
Labs -HLA-B27, inflammatory markers etc.
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11
Q

What are some treatment options for JIA?

A
  • Intra-articular Steroids
  • Disease Modifiying Anti-Inflammatory drugs (DMARDs) e.g. methotrexate.
  • Biologics e.g. Anti-TNF agents
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12
Q

What are some consequences of uveitis associated with JIA?

A
Red eyes
Headache
Reduced vision
Cataracts
Glaucoma
Blindness
Chronic uveitis
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13
Q

What is the treatment for uveitis?

A

Topical steroids
Systemic steroids if severe
DMARD and biologics if poor response

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14
Q

What are some complications of JIA?

A
Poor growth
Localised growth disturbances
Micrognathia - undersized lower jaw. 
Contractures - permanent tightening of tissues. 
Occular complications
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