International Journal of Hematology-Oncology and Stem Cell Research (Oct 2017)

Rare Presentation of Refractory Thrombotic Thrombocytopenic Purpura: Jejunal Stricture

  • Prabath K. Abeysundara,
  • Inoshi Atukorala,
  • K. P. C. Dalpatadu,
  • Karthiha Balendran,
  • M. D. S. A. Dilrukshi,
  • G M O Fernando

Journal volume & issue
Vol. 11, no. 4

Abstract

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Thrombotic thrombocytopenic purpura is a rare thrombotic disease characterized by episodes of thrombocytopenia and microangiopathic hemolytic anemia due to disseminated microvascular thrombosis. Thrombotic thrombocytopenic purpura was first described in 1924 by Moschowitz as a disease presenting with a pentad of signs and symptoms (anemia, thrombocytopenia, fever, hemiparesis and hematuria). Previous studies have described atypical manifestations of thrombotic thrombocytopenic purpura such as hemolysis, anemia and thrombosis.

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