Juvenile Idiopathic Disease, Told, Part II Flashcards
general characteristics RF + polyarticular JIA
> 8 y.o F>M
clinical features RF+ polyarticular JIA
polyarthritis of any joint (small joints common) rheumatoid nodules vasculitis
labs in RF + polyarticular JIA
ESR inc CBC anemia RF high titer + ANA positive HLA DR4 + XR early erosive changes
course and prognosis RF + polyarticular JIA
persistent- serious joint destruction and poor function
long term hazards of polyarticlar RF + JIA
C1 C2 subluxation aortic insufficiency and amyloidosis
management RF+ polyarticular JIA
splinting PT and OT NSAIDs DMARDs biologic agents surgical intervention
Tx JIA
NSAIDs Gold sulfasalazine antiTNF agents (Etanercept) antimalarials, MTX, azathiprine, steroids
following finding in 10 y.0 M
also has iritis and cc SI pain
pauciarticular subtype II JIA (spondylosis)
8 y.o F presents with this
pauciarticular subtype III psoriatic
child presents with this rash and painful joints
JRA rash
looks like allergy, but not