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A Metastatic Signet Ring Cell Carcinoma Presented as Acquired Thrombotic Thrombocytopenic Purpura: A Case Report
Microangiopathic hemolytic anemia (MAHA) may occur as a paraneoplastic syndrome in some solid tumors, but MAHA accompanied by signet ring cell carcinoma (SRCC) of an unknown origin is very rare. We report a patient who presented with an acute onset of Coombs negative hemolytic anemia and frequent sc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155867/ https://www.ncbi.nlm.nih.gov/pubmed/32300416 http://dx.doi.org/10.14740/jh386e |
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author | Eisa, Noha Nasef, Khalid Emarah, Ziad Fattah, Marwa Mohamed Abdel Shamaa, Sameh |
author_facet | Eisa, Noha Nasef, Khalid Emarah, Ziad Fattah, Marwa Mohamed Abdel Shamaa, Sameh |
author_sort | Eisa, Noha |
collection | PubMed |
description | Microangiopathic hemolytic anemia (MAHA) may occur as a paraneoplastic syndrome in some solid tumors, but MAHA accompanied by signet ring cell carcinoma (SRCC) of an unknown origin is very rare. We report a patient who presented with an acute onset of Coombs negative hemolytic anemia and frequent schistocytes in the peripheral blood smear which are typical for MAHA as initial presentation of metastatic SRCC. Our patients fulfilled the criteria of thrombotic thrombocytopenic purpura (TTP) and received the specific treatment for TTP without improvement. |
format | Online Article Text |
id | pubmed-7155867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71558672020-04-16 A Metastatic Signet Ring Cell Carcinoma Presented as Acquired Thrombotic Thrombocytopenic Purpura: A Case Report Eisa, Noha Nasef, Khalid Emarah, Ziad Fattah, Marwa Mohamed Abdel Shamaa, Sameh J Hematol Case Report Microangiopathic hemolytic anemia (MAHA) may occur as a paraneoplastic syndrome in some solid tumors, but MAHA accompanied by signet ring cell carcinoma (SRCC) of an unknown origin is very rare. We report a patient who presented with an acute onset of Coombs negative hemolytic anemia and frequent schistocytes in the peripheral blood smear which are typical for MAHA as initial presentation of metastatic SRCC. Our patients fulfilled the criteria of thrombotic thrombocytopenic purpura (TTP) and received the specific treatment for TTP without improvement. Elmer Press 2018-05 2018-05-10 /pmc/articles/PMC7155867/ /pubmed/32300416 http://dx.doi.org/10.14740/jh386e Text en Copyright 2018, Eisa et al. http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Eisa, Noha Nasef, Khalid Emarah, Ziad Fattah, Marwa Mohamed Abdel Shamaa, Sameh A Metastatic Signet Ring Cell Carcinoma Presented as Acquired Thrombotic Thrombocytopenic Purpura: A Case Report |
title | A Metastatic Signet Ring Cell Carcinoma Presented as Acquired Thrombotic Thrombocytopenic Purpura: A Case Report |
title_full | A Metastatic Signet Ring Cell Carcinoma Presented as Acquired Thrombotic Thrombocytopenic Purpura: A Case Report |
title_fullStr | A Metastatic Signet Ring Cell Carcinoma Presented as Acquired Thrombotic Thrombocytopenic Purpura: A Case Report |
title_full_unstemmed | A Metastatic Signet Ring Cell Carcinoma Presented as Acquired Thrombotic Thrombocytopenic Purpura: A Case Report |
title_short | A Metastatic Signet Ring Cell Carcinoma Presented as Acquired Thrombotic Thrombocytopenic Purpura: A Case Report |
title_sort | metastatic signet ring cell carcinoma presented as acquired thrombotic thrombocytopenic purpura: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155867/ https://www.ncbi.nlm.nih.gov/pubmed/32300416 http://dx.doi.org/10.14740/jh386e |
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