8 results
diagnosis rheumatology disease stills syndrome aosd activation adult dermatology diagnossi hematology kawasaki kd macrophage major mas minor onset pediatrics shock
Adult Onset Still's Disease - Yamaguchi Criteria Major criteria: - Fever >= 39C lasting >= 1 weeks
Major criteria ... - Typical skin rash ... : maculopapular, ... non-pruritic, salmon-pink rash ... polyarteritis nodosa #AdultOnset
Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Definition: • Severe adverse drug reaction, characterized by
Systemic Symptoms (DRESS ... extensive skin rash ... • Maculopapular ... Criteria for Diagnosis ... disease: symptomatic treatment
Adult-Onset Still's Disease (AOSD) Rare inflammatory disorder of unknown etiology, difficult to diagnose because of heterogenous presentation.
salmon-colored maculopapular ... rash, arthritis ... BrighamChiefs #AdultOnset ... rheumatology #diagnosis #management ... #treatment
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
arthritis, Skin rash ... Prunelle Getten #AdultOnset ... Disease #diagnosis #management ... #treatment #rheumatology
Adult Onset Still's Disease Systemic inflammation with urticarial rash. Rash: • Nonpruritic, evanescent (correlates with time of
with urticarial rash ... nonpruritic macular or maculopapular ... Treatment - Mild ... : NSAIDS Treatment ... #rheumatology #management
Kawasaki Disease (KD) - Diagnosis and Management Summary Kawasaki Disease (KD) is the most common vasculitis of
Diagnosis and Management ... Conjunctivitis, Mucositis, Rash ... Diagnostic Criteria ... Polymorphous rash ... #treatment
Streptococcal Toxic Shock Syndrome (STSS) Complication of invasive GAS disease characterized by shock & MOF → occurs
fasc Diagnostic Criteria ... erythematous macular rash ... necrosis STSS Treatment ... Syndrome #STSS #treatment ... #management #diagnosis
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Petechial or purpuric rash ... Histopathologic criteria ... Treatment: • Corticosteroids ... Syndrome #Diagnosis #Management
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