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Hemolytic uremic syndrome associated with Plasmodium vivax malaria successfully treated with plasma exchange
We report a case of hemolytic uremic syndrome (HUS) in an adult patient with Plasmodium vivax malaria. The patient presented with worsening anemia, persistent thrombocytopenia and acute kidney injury. HUS was diagnosed based on the high serum lactate dehydrogenase, elevated reticulocyte count and pr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927189/ https://www.ncbi.nlm.nih.gov/pubmed/24574629 http://dx.doi.org/10.4103/0971-4065.125054 |
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author | Keskar, V. S. Jamale, T. E. Hase, N. K. |
author_facet | Keskar, V. S. Jamale, T. E. Hase, N. K. |
author_sort | Keskar, V. S. |
collection | PubMed |
description | We report a case of hemolytic uremic syndrome (HUS) in an adult patient with Plasmodium vivax malaria. The patient presented with worsening anemia, persistent thrombocytopenia and acute kidney injury. HUS was diagnosed based on the high serum lactate dehydrogenase, elevated reticulocyte count and presence of schistocytes on peripheral blood smear. Kidney biopsy showed features of thrombotic microangiopathy. Complete hematological remission was achieved after five sessions of therapeutic plasma exchange. Renal function partially recovered and stabilized at discharge. Vivax malaria, generally considered benign, may be rarely associated with HUS. |
format | Online Article Text |
id | pubmed-3927189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-39271892014-02-26 Hemolytic uremic syndrome associated with Plasmodium vivax malaria successfully treated with plasma exchange Keskar, V. S. Jamale, T. E. Hase, N. K. Indian J Nephrol Case Report We report a case of hemolytic uremic syndrome (HUS) in an adult patient with Plasmodium vivax malaria. The patient presented with worsening anemia, persistent thrombocytopenia and acute kidney injury. HUS was diagnosed based on the high serum lactate dehydrogenase, elevated reticulocyte count and presence of schistocytes on peripheral blood smear. Kidney biopsy showed features of thrombotic microangiopathy. Complete hematological remission was achieved after five sessions of therapeutic plasma exchange. Renal function partially recovered and stabilized at discharge. Vivax malaria, generally considered benign, may be rarely associated with HUS. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC3927189/ /pubmed/24574629 http://dx.doi.org/10.4103/0971-4065.125054 Text en Copyright: © Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Keskar, V. S. Jamale, T. E. Hase, N. K. Hemolytic uremic syndrome associated with Plasmodium vivax malaria successfully treated with plasma exchange |
title | Hemolytic uremic syndrome associated with Plasmodium vivax malaria successfully treated with plasma exchange |
title_full | Hemolytic uremic syndrome associated with Plasmodium vivax malaria successfully treated with plasma exchange |
title_fullStr | Hemolytic uremic syndrome associated with Plasmodium vivax malaria successfully treated with plasma exchange |
title_full_unstemmed | Hemolytic uremic syndrome associated with Plasmodium vivax malaria successfully treated with plasma exchange |
title_short | Hemolytic uremic syndrome associated with Plasmodium vivax malaria successfully treated with plasma exchange |
title_sort | hemolytic uremic syndrome associated with plasmodium vivax malaria successfully treated with plasma exchange |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927189/ https://www.ncbi.nlm.nih.gov/pubmed/24574629 http://dx.doi.org/10.4103/0971-4065.125054 |
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