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Atypical Hemolytic Uremic Syndrome After Liver Transplant Treated With Eculizumab

Thrombotic microangiopathies (TMA) are a group of serious conditions that are characterized by microangiopathic hemolytic anemia and thrombocytopenia, and are often associated with acute kidney injury as well as neurologic abnormalities. There are multiple causes of TMA. TMA in a transplant patient...

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Detalles Bibliográficos
Autores principales: Bhatti, Sundus, Alghamdi, Mohammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430551/
https://www.ncbi.nlm.nih.gov/pubmed/32821578
http://dx.doi.org/10.7759/cureus.9230
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author Bhatti, Sundus
Alghamdi, Mohammed
author_facet Bhatti, Sundus
Alghamdi, Mohammed
author_sort Bhatti, Sundus
collection PubMed
description Thrombotic microangiopathies (TMA) are a group of serious conditions that are characterized by microangiopathic hemolytic anemia and thrombocytopenia, and are often associated with acute kidney injury as well as neurologic abnormalities. There are multiple causes of TMA. TMA in a transplant patient is often attributed to calcineurin inhibitor (CNI) use and is usually treated with discontinuation of the drug. We report a case of TMA in a liver transplant patient who did not respond to CNI discontinuation or plasmapheresis but had great response to shorter than usual course of eculizumab. Eculizumab is a monoclonal antibody that prevents c5 cleavage and indirectly inhibits the formation of the membrane attack complex. Clinical response was sustained for nine months after discontinuation of eculizumab.
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spelling pubmed-74305512020-08-18 Atypical Hemolytic Uremic Syndrome After Liver Transplant Treated With Eculizumab Bhatti, Sundus Alghamdi, Mohammed Cureus Allergy/Immunology Thrombotic microangiopathies (TMA) are a group of serious conditions that are characterized by microangiopathic hemolytic anemia and thrombocytopenia, and are often associated with acute kidney injury as well as neurologic abnormalities. There are multiple causes of TMA. TMA in a transplant patient is often attributed to calcineurin inhibitor (CNI) use and is usually treated with discontinuation of the drug. We report a case of TMA in a liver transplant patient who did not respond to CNI discontinuation or plasmapheresis but had great response to shorter than usual course of eculizumab. Eculizumab is a monoclonal antibody that prevents c5 cleavage and indirectly inhibits the formation of the membrane attack complex. Clinical response was sustained for nine months after discontinuation of eculizumab. Cureus 2020-07-16 /pmc/articles/PMC7430551/ /pubmed/32821578 http://dx.doi.org/10.7759/cureus.9230 Text en Copyright © 2020, Bhatti et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Allergy/Immunology
Bhatti, Sundus
Alghamdi, Mohammed
Atypical Hemolytic Uremic Syndrome After Liver Transplant Treated With Eculizumab
title Atypical Hemolytic Uremic Syndrome After Liver Transplant Treated With Eculizumab
title_full Atypical Hemolytic Uremic Syndrome After Liver Transplant Treated With Eculizumab
title_fullStr Atypical Hemolytic Uremic Syndrome After Liver Transplant Treated With Eculizumab
title_full_unstemmed Atypical Hemolytic Uremic Syndrome After Liver Transplant Treated With Eculizumab
title_short Atypical Hemolytic Uremic Syndrome After Liver Transplant Treated With Eculizumab
title_sort atypical hemolytic uremic syndrome after liver transplant treated with eculizumab
topic Allergy/Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430551/
https://www.ncbi.nlm.nih.gov/pubmed/32821578
http://dx.doi.org/10.7759/cureus.9230
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