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Mycobacterium avium Complex-Associated Hemophagocytic Lymphohistiocytosis in a Sickle Cell Patient: An Unusual Fatal Association
Hemophagocytic lymphohistiocytosis (HLH) is a rare hyperinflammatory syndrome, characterized clinically by fever, splenomegaly, cytopenia, and high ferritin. Infectious causes have been associated with secondary HLH, with viruses being the most common. We report a case of Mycobacterium avium complex...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670468/ https://www.ncbi.nlm.nih.gov/pubmed/23762672 http://dx.doi.org/10.1155/2013/291518 |
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author | Chamsi-Pasha, Mohammed A. R. Alraies, M. Chadi Alraiyes, Abdul Hamid Hsi, Eric D. |
author_facet | Chamsi-Pasha, Mohammed A. R. Alraies, M. Chadi Alraiyes, Abdul Hamid Hsi, Eric D. |
author_sort | Chamsi-Pasha, Mohammed A. R. |
collection | PubMed |
description | Hemophagocytic lymphohistiocytosis (HLH) is a rare hyperinflammatory syndrome, characterized clinically by fever, splenomegaly, cytopenia, and high ferritin. Infectious causes have been associated with secondary HLH, with viruses being the most common. We report a case of Mycobacterium avium complex-associated HLH in a sickle cell anemia patient. To the best of our knowledge, this association has never been reported in sickle cell anemia. |
format | Online Article Text |
id | pubmed-3670468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-36704682013-06-12 Mycobacterium avium Complex-Associated Hemophagocytic Lymphohistiocytosis in a Sickle Cell Patient: An Unusual Fatal Association Chamsi-Pasha, Mohammed A. R. Alraies, M. Chadi Alraiyes, Abdul Hamid Hsi, Eric D. Case Rep Hematol Case Report Hemophagocytic lymphohistiocytosis (HLH) is a rare hyperinflammatory syndrome, characterized clinically by fever, splenomegaly, cytopenia, and high ferritin. Infectious causes have been associated with secondary HLH, with viruses being the most common. We report a case of Mycobacterium avium complex-associated HLH in a sickle cell anemia patient. To the best of our knowledge, this association has never been reported in sickle cell anemia. Hindawi Publishing Corporation 2013 2013-05-16 /pmc/articles/PMC3670468/ /pubmed/23762672 http://dx.doi.org/10.1155/2013/291518 Text en Copyright © 2013 Mohammed A. R. Chamsi-Pasha et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Chamsi-Pasha, Mohammed A. R. Alraies, M. Chadi Alraiyes, Abdul Hamid Hsi, Eric D. Mycobacterium avium Complex-Associated Hemophagocytic Lymphohistiocytosis in a Sickle Cell Patient: An Unusual Fatal Association |
title |
Mycobacterium avium Complex-Associated Hemophagocytic Lymphohistiocytosis in a Sickle Cell Patient: An Unusual Fatal Association |
title_full |
Mycobacterium avium Complex-Associated Hemophagocytic Lymphohistiocytosis in a Sickle Cell Patient: An Unusual Fatal Association |
title_fullStr |
Mycobacterium avium Complex-Associated Hemophagocytic Lymphohistiocytosis in a Sickle Cell Patient: An Unusual Fatal Association |
title_full_unstemmed |
Mycobacterium avium Complex-Associated Hemophagocytic Lymphohistiocytosis in a Sickle Cell Patient: An Unusual Fatal Association |
title_short |
Mycobacterium avium Complex-Associated Hemophagocytic Lymphohistiocytosis in a Sickle Cell Patient: An Unusual Fatal Association |
title_sort | mycobacterium avium complex-associated hemophagocytic lymphohistiocytosis in a sickle cell patient: an unusual fatal association |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670468/ https://www.ncbi.nlm.nih.gov/pubmed/23762672 http://dx.doi.org/10.1155/2013/291518 |
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