6 results
diagnosis symptoms hematology rheumatology syndrome vasculitis activation ascorbicacid behcet causes coagulation dic disease disseminated henochscholeinpurpura iga intravascular mas nutrition pan
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
easy bruising to purpura ... mucosal bleeding (Petechial ... or purpuric rash ... 5000 to 10,000 ng/mL ... Syndrome #Diagnosis #Management
Scurvy (Vitamin C Deficiency) - Diagnosis and Management Vitamin C is required for hydroxylation of proline residues
Diagnosis and Management ... poor nutrition Clinical ... • Purpura • Perifollicular ... • Petechiae, purpura ... Henoch-Schonlein purpura
Polyarteritis Nodosa (PAN): Pathogenesis and Clinical Findings Medical Comorbidities Malignancies (most commonly hairy-cell leukemia) Immunogenetic Predisposition: patient is
Pathogenesis and Clinical ... endothelial cells - Palpable ... or necrotic purpura ... PolyarteritisNodosa #Pathophysiology ... #Diagnosis #Signs
IgA Vasculitis – Henoch Scholein Purpura: Pathogenesis and Clinical Findings - Infectious Agents - 50% have
Henoch Scholein Purpura ... Pathogenesis and Clinical ... chemotaxis and macrophage ... and ankles) #HSP ... #Diagnosis #Signs
Disseminated Intravascular Coagulation (DIC) Overview Increased Clotting and Consumption of Clotting Factors Findings: • Bleeding • Recent history
protein C and S Pathophysiology ... organ damage Clinical ... • Purpura • ... Palpable variants ... Hemorrhagic bullae • Purpura
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... multiforme-like lesions, palpable ... purpura, Pathergy ... Syndrome #diagnosis #management ... #signs #symptoms
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