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Oxaliplatin-Induced Thrombotic Microangiopathy in a Patient with Stage IV Gallbladder Carcinoma: Primary Association or Multiple Hits?

Thrombotic microangiopathies (TMA) include a variety of vascular disorders characterized by the presence of microthrombi, coagulopathy by platelet activation and consumption, and systemic damage. The most frequent secondary causes are infections and some medications. However, the presence of chemoth...

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Autores principales: Fuentes-Lacouture, María Cynthia, Barrera-Garavito, Edgar Camilo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590773/
https://www.ncbi.nlm.nih.gov/pubmed/33173484
http://dx.doi.org/10.1159/000510307
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author Fuentes-Lacouture, María Cynthia
Barrera-Garavito, Edgar Camilo
author_facet Fuentes-Lacouture, María Cynthia
Barrera-Garavito, Edgar Camilo
author_sort Fuentes-Lacouture, María Cynthia
collection PubMed
description Thrombotic microangiopathies (TMA) include a variety of vascular disorders characterized by the presence of microthrombi, coagulopathy by platelet activation and consumption, and systemic damage. The most frequent secondary causes are infections and some medications. However, the presence of chemotherapeutic agents is not so common, and the induction of TMA by oxaliplatin is poorly understood, with few published case reports. We present the case of a patient with a history of gallbladder carcinoma, in whom findings compatible with TMA were documented, and with a temporal and sole relation to oxaliplatin.
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spelling pubmed-75907732020-11-09 Oxaliplatin-Induced Thrombotic Microangiopathy in a Patient with Stage IV Gallbladder Carcinoma: Primary Association or Multiple Hits? Fuentes-Lacouture, María Cynthia Barrera-Garavito, Edgar Camilo Case Rep Oncol Case Report Thrombotic microangiopathies (TMA) include a variety of vascular disorders characterized by the presence of microthrombi, coagulopathy by platelet activation and consumption, and systemic damage. The most frequent secondary causes are infections and some medications. However, the presence of chemotherapeutic agents is not so common, and the induction of TMA by oxaliplatin is poorly understood, with few published case reports. We present the case of a patient with a history of gallbladder carcinoma, in whom findings compatible with TMA were documented, and with a temporal and sole relation to oxaliplatin. S. Karger AG 2020-09-29 /pmc/articles/PMC7590773/ /pubmed/33173484 http://dx.doi.org/10.1159/000510307 Text en Copyright © 2020 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
Fuentes-Lacouture, María Cynthia
Barrera-Garavito, Edgar Camilo
Oxaliplatin-Induced Thrombotic Microangiopathy in a Patient with Stage IV Gallbladder Carcinoma: Primary Association or Multiple Hits?
title Oxaliplatin-Induced Thrombotic Microangiopathy in a Patient with Stage IV Gallbladder Carcinoma: Primary Association or Multiple Hits?
title_full Oxaliplatin-Induced Thrombotic Microangiopathy in a Patient with Stage IV Gallbladder Carcinoma: Primary Association or Multiple Hits?
title_fullStr Oxaliplatin-Induced Thrombotic Microangiopathy in a Patient with Stage IV Gallbladder Carcinoma: Primary Association or Multiple Hits?
title_full_unstemmed Oxaliplatin-Induced Thrombotic Microangiopathy in a Patient with Stage IV Gallbladder Carcinoma: Primary Association or Multiple Hits?
title_short Oxaliplatin-Induced Thrombotic Microangiopathy in a Patient with Stage IV Gallbladder Carcinoma: Primary Association or Multiple Hits?
title_sort oxaliplatin-induced thrombotic microangiopathy in a patient with stage iv gallbladder carcinoma: primary association or multiple hits?
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590773/
https://www.ncbi.nlm.nih.gov/pubmed/33173484
http://dx.doi.org/10.1159/000510307
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