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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2020
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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. |
format | Online Article Text |
id | pubmed-7430551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT bhattisundus atypicalhemolyticuremicsyndromeafterlivertransplanttreatedwitheculizumab AT alghamdimohammed atypicalhemolyticuremicsyndromeafterlivertransplanttreatedwitheculizumab |