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diagnosis syndrome behcets classification differential oncology stills treatment adult adultonset aosd behcet criteria cryofibrinogenemia dermatology hodgkins lymphoma monoclonal onset paraproteinemias
Behcet's Syndrome - Diagnosis Diagnostic Criteria for Behget's Syndrome (International Study Group for Behget's Disease): • Recurrent,
Group for Behget's Disease ... disease: Uveitis ... or retinal vasculitis ... , retinal vasculitis ... Diagnosis #criteria #rheumatology
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Adult-Onset Still's Disease ... autoinflammatory diseases ... • Ocular: uveitis ... #diagnosis #management ... #treatment #rheumatology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
ulceration • Ocular ... (panuveitis, retinal ... : Giant retinal ... Syndrome #diagnosis #management ... signs #symptoms #rheumatology
Susac Syndrome - Clinical Triad - Central nervous system dysfunction - Branch retinal artery occlusion -
dysfunction - Branch retinal ... - Recurrent disease ... fluorescein from retinal ... Triad #Diagnosis #Management ... #Rheumatology
Behcet's Syndrome - Treatment Ulcers: • Treatment: Topical steroids • Prevention: Colchicine • Azathioprine for refractory disease Arthritis:
for refractory disease ... refractory lesions Ocular ... disease: • Early ... Syndrome #Treatment #management ... #pharmacology #rheumatology
Cryofibrinogenemia Summary Cryofibrinogenemia Epidemiology: • 40-70 years with a modest female predominance Cryofibrinogenemia: • The precipitation of a
with autoimmune diseases ... pulmonary emboli, and ocular ... thrombi including retinal ... Cryofibrinogenemia #diagnosis #rheumatology ... #hematology
Vasculitis and Vasculitides - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions •
, and ocular inflammation ... ulcers, cutaneous, ocular ... Syndrome: - Ocular ... Eye -> retinopathy ... differential #diagnosis #rheumatology
Paraproteinemias Entities That Can Feature A Monoclonal Protein/M Component: • MM • WM • MGUS • MGCS • MGRS • Splenic Marginal Zone
• Heavy Chain disease ... Hypergammaglobulinemic macular ... Sneddon-Wilkinson disease ... vascular beds-renal, retinal ... Paraproteinemias #Hematology
Adult Onset Still's Disease Systemic inflammation with urticarial rash. Rash: • Nonpruritic, evanescent (correlates with time of
Onset Still's Disease ... A nonpruritic macular ... onset #Stills #disease ... AOSD #diagnosis #rheumatology ... #management
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
sites such as the collar ... osteoarticular and skin disease ... SAPHO #Syndrome #Rheumatology ... #diagnosis #management ... #Dermatology
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