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Case Report
Thrombotic Microangiopathy and Low ADAMTS 13: Case Report and Review of the Literature
Author(s): Zakaria Almuwaqqat, Saad Ali, Abduljalil Elfasi, Harvey Freidman and Afsin OktayZakaria Almuwaqqat, Saad Ali, Abduljalil Elfasi, Harvey Freidman and Afsin Oktay
Background: Thrombotic Microangiopathy (TMA) is a multi-organ dysfunction syndrome characterized by microvascular thrombosis, thrombocytopenia and hemolytic anemia with diverse etiologies ranging from primary Thrombotic thrombocytopenic purura (TTP) and Hemolytic uremic syndrome (HUS) to secondary phenomena to medications, severe uncontrolled hypertension and autoimmune disorders i.e Scleroderma renal crises, catastrophic antiphospholipid syndrome and pre-eclampsia, prompt diagnosis, identification of potential etiologies and treatment are essential steps for reducing morbidity and mortality.
Case Report: We describe a case of a 34-year-old man who presented with features of advanced renal impairment, severe uncontrolled hypertension and thrombotic microangiopathy, overall clinical picture was most consistent with malignant hypertension and hy.. Read More»
DOI:
10.4172/2157-7099.1000359
Journal of Cytology & Histology received 2334 citations as per Google Scholar report