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diagnosis dermatology dress drugreaction eosinophilia symptoms hematology anemia antinxp2 antinxp2dm aplastic arteritis behcet dermatomyositis disease gangrenosum gca giantcell hemeonc hemophagocytic
Tinea Versicolor: Scaly well demarcated patches caused by fungal skin infection. Charlie Goldberg, M.D. - UCSD Catalog
demarcated patches caused ... by fungal skin ... Images #Clinical ... #Photo #Dermatology ... #SkinRash #Tinea
Drug Reaction with Eosinophilia and Systemic Signs (DRESS Syndrome): Formerly known as drug hypersensitivity reaction, DRESS represents
Eosinophilia and Systemic Signs ... medication (in this case ... #Dermatology #SkinRash ... Eosinophilia #Legs #Photo ... #UCSDH
Drug Reaction with Eosinophilia and Systemic Signs (DRESS Syndrome): Formerly known as drug hypersensitivity reaction, DRESS represents
Eosinophilia and Systemic Signs ... medication (in this case ... #Dermatology #SkinRash ... Eosinophilia #Photo ... #UCSDH
Pyoderma Gangrenosum: Autoimmune disorder resulting in a vasculitis which causes slowly progressive ulceration of the skin.
vasculitis which causes ... ulceration of the skin ... Images #Clinical ... #Photo #Dermatology ... #SkinRash #Pyoderma
Drug Reaction with Eosinophilia and Systemic Signs (DRESS Syndrome): Formerly known as drug hypersensitivity reaction, DRESS represents
Eosinophilia and Systemic Signs ... medication (in this case ... #Dermatology #SkinRash ... Eosinophilia #Trunk #Photo ... #UCSDH
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... (Clinical Dx). ... #diagnosis #management ... #signs #symptoms ... #rheumatology #
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
Diagnosis and Management ... renal failure Clinical ... nodes: 13-15%, skin ... Sarcoidosis #Diagnosis #Management ... #Signs #Symptoms
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
Rheumatic pain Clinical ... Diagnosis: • A clinical ... Rule out other causes ... #Rheumatology # ... 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 ... Headaches • Pale skin ... and petechiae Causes ... Anemia #oncology #hematology ... #diagnosis #management
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
Diagnosis = clinical ... systemic sx + signs ... required due to skip ... them, but urgent rheumatology ... Symptoms #Diagnosis #Management
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