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A Case of Thrombotic Thrombocytopenic Purpura without Pathognomonic Schistocytes

Patients diagnosed with thrombotic thrombocytopenic purpura (TTP) typically present with microangiopathic hemolytic anemia (MAHA) and thrombocytopenia; these two clinical manifestations were often believed to be essential indicators of TTP. However, such indicators are not always present in every ca...

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Detalles Bibliográficos
Autores principales: Yu, Kevin, Yan, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8167742/
https://www.ncbi.nlm.nih.gov/pubmed/33924287
http://dx.doi.org/10.3390/clinpract11020033
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author Yu, Kevin
Yan, Min
author_facet Yu, Kevin
Yan, Min
author_sort Yu, Kevin
collection PubMed
description Patients diagnosed with thrombotic thrombocytopenic purpura (TTP) typically present with microangiopathic hemolytic anemia (MAHA) and thrombocytopenia; these two clinical manifestations were often believed to be essential indicators of TTP. However, such indicators are not always present in every case. Here, we present a patient affected by TTP but showing no distinctive schistocytes on blood smear review. TTP was diagnosed through a critically low level of a disintegrin and metalloproteinase with thrombospondin type 1 motif, member 13 (ADAMTS13) activity. Awareness of such an atypical presentation of TTP is essential for timely treatment to prevent serious and even fatal outcomes for patients.
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spelling pubmed-81677422021-06-02 A Case of Thrombotic Thrombocytopenic Purpura without Pathognomonic Schistocytes Yu, Kevin Yan, Min Clin Pract Case Report Patients diagnosed with thrombotic thrombocytopenic purpura (TTP) typically present with microangiopathic hemolytic anemia (MAHA) and thrombocytopenia; these two clinical manifestations were often believed to be essential indicators of TTP. However, such indicators are not always present in every case. Here, we present a patient affected by TTP but showing no distinctive schistocytes on blood smear review. TTP was diagnosed through a critically low level of a disintegrin and metalloproteinase with thrombospondin type 1 motif, member 13 (ADAMTS13) activity. Awareness of such an atypical presentation of TTP is essential for timely treatment to prevent serious and even fatal outcomes for patients. MDPI 2021-04-13 /pmc/articles/PMC8167742/ /pubmed/33924287 http://dx.doi.org/10.3390/clinpract11020033 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Yu, Kevin
Yan, Min
A Case of Thrombotic Thrombocytopenic Purpura without Pathognomonic Schistocytes
title A Case of Thrombotic Thrombocytopenic Purpura without Pathognomonic Schistocytes
title_full A Case of Thrombotic Thrombocytopenic Purpura without Pathognomonic Schistocytes
title_fullStr A Case of Thrombotic Thrombocytopenic Purpura without Pathognomonic Schistocytes
title_full_unstemmed A Case of Thrombotic Thrombocytopenic Purpura without Pathognomonic Schistocytes
title_short A Case of Thrombotic Thrombocytopenic Purpura without Pathognomonic Schistocytes
title_sort case of thrombotic thrombocytopenic purpura without pathognomonic schistocytes
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8167742/
https://www.ncbi.nlm.nih.gov/pubmed/33924287
http://dx.doi.org/10.3390/clinpract11020033
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