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Rare Presentation of Refractory Thrombotic Thrombocytopenic Purpura: Jejunal Stricture

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 wit...

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Autores principales: Abeysundara, Prabath K., Athukorala, Inoshi, Dalpatadu, K.P.C., Balendran, Karthiha, Dilrukshi, M.D.S.A., Fernando, GMO
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767289/
https://www.ncbi.nlm.nih.gov/pubmed/29340125
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author Abeysundara, Prabath K.
Athukorala, Inoshi
Dalpatadu, K.P.C.
Balendran, Karthiha
Dilrukshi, M.D.S.A.
Fernando, GMO
author_facet Abeysundara, Prabath K.
Athukorala, Inoshi
Dalpatadu, K.P.C.
Balendran, Karthiha
Dilrukshi, M.D.S.A.
Fernando, GMO
author_sort Abeysundara, Prabath K.
collection PubMed
description 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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spelling pubmed-57672892018-01-16 Rare Presentation of Refractory Thrombotic Thrombocytopenic Purpura: Jejunal Stricture Abeysundara, Prabath K. Athukorala, Inoshi Dalpatadu, K.P.C. Balendran, Karthiha Dilrukshi, M.D.S.A. Fernando, GMO Int J Hematol Oncol Stem Cell Res Case Report 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. Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2017-10-01 /pmc/articles/PMC5767289/ /pubmed/29340125 Text en Copyright : © International Journal of Hematology-Oncology and Stem Cell Research & Tehran University of Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Abeysundara, Prabath K.
Athukorala, Inoshi
Dalpatadu, K.P.C.
Balendran, Karthiha
Dilrukshi, M.D.S.A.
Fernando, GMO
Rare Presentation of Refractory Thrombotic Thrombocytopenic Purpura: Jejunal Stricture
title Rare Presentation of Refractory Thrombotic Thrombocytopenic Purpura: Jejunal Stricture
title_full Rare Presentation of Refractory Thrombotic Thrombocytopenic Purpura: Jejunal Stricture
title_fullStr Rare Presentation of Refractory Thrombotic Thrombocytopenic Purpura: Jejunal Stricture
title_full_unstemmed Rare Presentation of Refractory Thrombotic Thrombocytopenic Purpura: Jejunal Stricture
title_short Rare Presentation of Refractory Thrombotic Thrombocytopenic Purpura: Jejunal Stricture
title_sort rare presentation of refractory thrombotic thrombocytopenic purpura: jejunal stricture
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767289/
https://www.ncbi.nlm.nih.gov/pubmed/29340125
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