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diagnosis hematology photo drugreaction eosinophilia syndrome ucsdh alopecia anemia aplastic coagulation common cvid dic hemeonc hemophagocytic hlh hypogammaglobulinemia immunodeficiency immunology
Drug Reaction with Eosinophilia and Systemic Signs (DRESS Syndrome): Formerly known as drug hypersensitivity reaction, DRESS represents
Systemic Signs (DRESS ... medication (in this case ... UCSD Catalog of Clinical ... Images #Clinical ... #Dermatology #SkinRash
Drug Reaction with Eosinophilia and Systemic Signs (DRESS Syndrome): Formerly known as drug hypersensitivity reaction, DRESS represents
Systemic Signs (DRESS ... medication (in this case ... UCSD Catalog of Clinical ... Images #Clinical ... #Dermatology #SkinRash
Secondary Disseminated Syphilis Case from my residency that @EstradaElJefe helped me publish in JGIM. One important finding
Secondary Disseminated ... Syphilis Case ... Syphilis #Secondary #Disseminated ... #Dermatology #Clinical ... #Photo #SkinRash
Tinea Versicolor (Pityriasis versicolor) NOT a dermatophyte infection Caused by saprophytic, lipid-dependent yeasts Clinical •
dermatophyte infection Caused ... lipid-dependent yeasts Clinical ... Tinea #Versicolor #Dermatology ... #SkinRash #Diagnosis ... #Management
Disseminated Intravascular Coagulation (DIC) Overview Increased Clotting and Consumption of Clotting Factors Findings: • Bleeding • Recent history
Disseminated Intravascular ... organ damage Clinical ... Treat primary cause ... #treatment #management ... #hematology
Drug Reaction with Eosinophilia and Systemic Signs (DRESS Syndrome): Formerly known as drug hypersensitivity reaction, DRESS represents
Systemic Signs (DRESS ... medication (in this case ... UCSD Catalog of Clinical ... Images #Clinical ... #Dermatology #SkinRash
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
to 8 years Clinical ... specifically immune thrombocytopenia ... and M panel Management ... DDX - Other causes ... #diagnosis #management
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Aplastic Anemia Clinical ... infections/fevers • Thrombocytopenia ... and petechiae Causes ... Anemia #oncology #hematology ... #diagnosis #management
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
recognition and management ... hyperinflammatory syndrome caused ... Clinical Presentation ... Cytopenias (anemia, thrombocytopenia ... #Hematology #HemeOnc
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