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disease dermatology stills symptoms syndrome adult adultonset antinxp2dm arteritis behcet dermatomyositis gca giantcell onset sapho temporal
Adult-Onset Still's Disease (AOSD) Rare inflammatory disorder of unknown etiology, difficult to diagnose because of heterogenous presentation.
Must rule out other ... low ferritin, arthritis ... #rheumatology # ... diagnosis #management ... #treatment
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
response to local skin ... test (this is a skin ... , AS Treatment: ... #management #signs ... #symptoms #rheumatology
Adult Onset Still's Disease Systemic inflammation with urticarial rash. Rash: • Nonpruritic, evanescent (correlates with time of
maculopapular skin ... Treatment - Mild ... Stills #disease #AOSD ... #diagnosis #rheumatology ... #management
Gout - Diagnosis and Management Summary 3 Conditions for Gout to Manifest: 1. Hyperuricemia 2. Monosodium urate deposition in
Gout - Diagnosis ... and Management ... frequent attacks • Arthritis ... #diagnosis #management ... #treatment #rheumatology
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
systemic sx + signs ... required due to skip ... Treatment of GCA ... them, but urgent rheumatology ... #Management
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
nonerosive inflammatory arthritis ... • Rule out other ... and lower jaw Treatment ... SAPHO #Syndrome #Rheumatology ... #diagnosis #management
Anti-NXP-2 Dermatomyositis What? DM with generalized subcutaneous edema Pts have more myalgias, more severe weakness, and an increased prevalence
chest (in a V-sign ... shoulders (in a shawl sign ... positive patients Treatment ... #diagnosis #management ... #rheumatology #
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