Primary Article
Thrombotic Thrombocytopenic Purpura—A Reevaluation
Abstract
Thrombotic thrombocytopenic purpura (TTP) is a syndrome in which thrombocytopenia, red cell fragmentation, and variable neurologic signs and symptoms are the defining features. Variations in the presentation and subsequent course of the syndrome are well known; two case histories illustrate possible variations. The role of fibrin formation and the relationship of TTP to other forms of vasculitis and disseminated intravascular coagulation are discussed, with emphasis upon appropriate selection of treatment.This content is limited to qualifying members.
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