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diagnosis rheumatology hematology aosd blood reactions syndrome treatment activation adult criteria dermatology macrophage major mas minor onset transfusion transfusions yamaguchi
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Adult-Onset Still's ... arthritis, Skin rash ... Prunelle Getten #AdultOnset ... #Stills #Disease ... #diagnosis #management
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 ... #Stills #Disease ... rheumatology #diagnosis #management
Adult Onset Still's Disease - Yamaguchi Criteria Major criteria: - Fever >= 39C lasting >= 1 weeks
Adult Onset Still's ... - Typical skin rash ... : maculopapular, ... polyarteritis nodosa #AdultOnset ... #Stills #Disease
Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Definition: • Severe adverse drug reaction, characterized by
Systemic Symptoms (DRESS ... extensive skin rash ... • Maculopapular ... withdrawal • Mild disease ... SinaiBmoreIMRes #DRESS
Adult Onset Still's Disease Systemic inflammation with urticarial rash. Rash: • Nonpruritic, evanescent (correlates with time of
Adult Onset Still's ... Disease Systemic ... nonpruritic macular or maculopapular ... #Adult #onset #Stills ... #rheumatology #management
Blood Product Transfusions One Pager Summary Type and screen - determines blood type and detects in recipient
/sx urticaria, maculopapular ... rash, pruritis, ... Graft Versus Host Disease ... Borrellia (Lyme disease ... Transfusions #diagnosis #management
Blood Transfusion Reactions Immune Mediated: • Febrile Non-Hemolytic Transfusion Reaction (FNHTR): Most common immune reaction to transfusion.
/sx urticaria, maculopapular ... rash, pruritis, ... Blood products contain ... of transfused products ... Transfusion #diagnosis #management
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
• Adult-onset Still ... disease • Systemic ... Petechial or purpuric rash ... Fibrin degradation products ... Syndrome #Diagnosis #Management
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