Systemic-onset juvenile idiopathic arthritis (Still's disease) Flashcards
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)
- 20%
_____ is the most common rheumatologic disease in childhood.
Juvenile idiopathic arthritis
M:F predominance of Stills disease?
M=F (all other JIA’s have female predominance)
By definition Juvenile idiopathic arthritis has an onset at age ____ or less.
16
What is pathogenesis of Still’s disease?
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
Which cytokine is the major driver of inflammation in Still’s disease?
IL-1
What are the diagnostic criteria for Still’s disease?
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%)
Histopath of Still’s disease:
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
What are the skin findings in stills disease?
- 90% will have transient evanescent, salmon pink, blanching eruption corresponding with fever spikes
- can also see persistent papules and plaques
Labs to check in Still disease:
- elevated ESR/CRP
- RF-negative
- ANA negative
Are RF and ANA in Stills disease negative or positive?
Both negative 95% of the time
Treatment for stills disease if mild? Mod-severe?
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
Prognosis of Still’s disease?
Arthritis resolves completely in 50%
- other 50% have chronic course w/ persistent arthtitis and systemic complications
Extensive arthritis or symptoms lasting > ______ amount of time is a/w poor prognosis in Stills disease.
6 months