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diagnosis differential hematology management naildisorders rheumatology common cryofibrinogenemia cryoglobulinemia cryoglobulins cvid gangrenosum hemeonc hemophagocytic hlh hypogammaglobulinemia immunodeficiency immunology lymphohistiocytosis papulosquamous
Nail Disorders - Primary and Systemic Causes - Differential Diagnosis Algorithm #NailDisorders #Primary #Secondary #Systemic #dermatology #Differential
Nail Disorders - ... Primary and Systemic ... NailDisorders #Primary #Secondary ... #Systemic #dermatology ... #causes
Nail Disorders secondary to Systemic Diseases Nail Fold Abnormality • SLE • Scleroderma • Dermatomyositis Koilonychia - Spoon-shaped
Nail Disorders secondary ... to Systemic Diseases ... #Secondary #dermatology ... Differential #Diagnosis #Algorithm ... #causes
Pyoderma Gangrenosum: Autoimmune disorder resulting in a vasculitis which causes slowly progressive ulceration of the skin.
Gangrenosum: Autoimmune disorder ... vasculitis which causes ... a number of systemic ... #Photo #Dermatology ... #SkinRash #Pyoderma
Papulosquamous Skin Rash - Differential Diagnosis Algorithm Erythrematous or violaceous papules & plaques with overlying scale •
polygonal, planar (flat-topped ... central clearing • Secondary ... Papulosquamous #SkinRash ... #dermatology #Differential ... #causes
Cryoglobulinemia Summary Cryoglobulins: • Cryoglobulins are Igs in the serum that precipitate in vitro at temperatures below
• They can cause ... Cryoglobulins Cause ... Syndrome: • Clinical ... Type III Often Secondary ... diagnosis #types #classification
Cryofibrinogenemia Summary Cryofibrinogenemia Epidemiology: • 40-70 years with a modest female predominance Cryofibrinogenemia: • The precipitation of a
cryoglobulinemia Associated Disorders ... processes: • Systemic ... Cryofibrinogenemia Clinical ... Diagnosis: • + Clinical ... cryoglobulins • Negative causes
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
Immunodeficiency disorder ... infection risk secondary ... to 8 years Clinical ... hemolytic anemia) • Systemic ... DDX - Other causes
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
hyperinflammatory syndrome caused ... of the immune system ... STX11, STXBP2 • Secondary ... Clinical Presentation ... malignancy, autoimmune disorder
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