Systemic-onset juvenile idiopathic arthritis (Still's disease) Flashcards

1
Q

Still’s disease accounts for ___ % of juvenile idiopathic arthritis and is one of the only ones that has skin findings (which is why dermatologists see this)

A
  • 20%
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2
Q

_____ is the most common rheumatologic disease in childhood.

A

Juvenile idiopathic arthritis

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3
Q

M:F predominance of Stills disease?

A

M=F (all other JIA’s have female predominance)

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4
Q

By definition Juvenile idiopathic arthritis has an onset at age ____ or less.

A

16

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5
Q

What is pathogenesis of Still’s disease?

A

autoinflammaotry syndrome (disorder of innate immune system) that leads to increased IL-1 production—> downstream effects., rather than an autoimmune disease of the adaptive immune system

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6
Q

Which cytokine is the major driver of inflammation in Still’s disease?

A

IL-1

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7
Q

What are the diagnostic criteria for Still’s disease?

A

High episodic feveers daily for >/= 2 weeks and documented to be daily for >/= 3 days (classically arises in late afternoon/early evening)

Plus one of the following:

  • transient, evanescent, salmon pink, blanching eruption (90%) that correlates with fevers and koebnerizes
  • generalized LAD
  • Hepatosplenomegaly
  • Serositis (pericarditis, pleuritis, perotinitis)
  • Symmetric polyarthritis > oligoarthritis (erosive in 20%)
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8
Q

Histopath of Still’s disease:

A

evanescent transient exanthem:

  • edema of superficial dermis
  • superficial, PV, and interstitial neutrophilic infiltrate in absence of vasculitis

Persistent papules/plaques

  • same as above + PK and superficially-scattered necrotic keratinocytes
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9
Q

What are the skin findings in stills disease?

A
  • 90% will have transient evanescent, salmon pink, blanching eruption corresponding with fever spikes
  • can also see persistent papules and plaques
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10
Q

Labs to check in Still disease:

A
  • elevated ESR/CRP

- RF-negative

- ANA negative

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11
Q

Are RF and ANA in Stills disease negative or positive?

A

Both negative 95% of the time

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12
Q

Treatment for stills disease if mild? Mod-severe?

A

For mild: NSAIDS +/- Hydroxychloroquine

For moderate-severe: Systemic steroids +/- steroid sparing immunosuppressants (MTX, TNF-a inhibitors)

  • IL-1 Receptor antagonists (Anakinra) and IL-6 receptor antagonists (rocilizumab) show promising results
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13
Q

Prognosis of Still’s disease?

A

Arthritis resolves completely in 50%

  • other 50% have chronic course w/ persistent arthtitis and systemic complications
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14
Q

Extensive arthritis or symptoms lasting > ______ amount of time is a/w poor prognosis in Stills disease.

A

6 months

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