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Hemophagocytic Lymphohistiocytosis Associated with Natural T-cell Leukemia
Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening syndrome of excessive immune activation. It can be triggered by a variety of events that disrupt immune homeostasis, infection being the most common of them. We report a case of a 36-year-old male diagnosed with HLH associated w...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6476604/ https://www.ncbi.nlm.nih.gov/pubmed/31058001 http://dx.doi.org/10.7759/cureus.4107 |
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author | Ricaurte, Frank R Kewan, Tariq Chadalavada, Pravallika Misbah, Seema Daw, Hamed |
author_facet | Ricaurte, Frank R Kewan, Tariq Chadalavada, Pravallika Misbah, Seema Daw, Hamed |
author_sort | Ricaurte, Frank R |
collection | PubMed |
description | Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening syndrome of excessive immune activation. It can be triggered by a variety of events that disrupt immune homeostasis, infection being the most common of them. We report a case of a 36-year-old male diagnosed with HLH associated with natural T-cell leukemia. The purpose of this report is to call attention to the clinical presentation, diagnosis, and treatment of HLH. |
format | Online Article Text |
id | pubmed-6476604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-64766042019-05-05 Hemophagocytic Lymphohistiocytosis Associated with Natural T-cell Leukemia Ricaurte, Frank R Kewan, Tariq Chadalavada, Pravallika Misbah, Seema Daw, Hamed Cureus Pathology Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening syndrome of excessive immune activation. It can be triggered by a variety of events that disrupt immune homeostasis, infection being the most common of them. We report a case of a 36-year-old male diagnosed with HLH associated with natural T-cell leukemia. The purpose of this report is to call attention to the clinical presentation, diagnosis, and treatment of HLH. Cureus 2019-02-20 /pmc/articles/PMC6476604/ /pubmed/31058001 http://dx.doi.org/10.7759/cureus.4107 Text en Copyright © 2019, Ricaurte 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 | Pathology Ricaurte, Frank R Kewan, Tariq Chadalavada, Pravallika Misbah, Seema Daw, Hamed Hemophagocytic Lymphohistiocytosis Associated with Natural T-cell Leukemia |
title | Hemophagocytic Lymphohistiocytosis Associated with Natural T-cell Leukemia |
title_full | Hemophagocytic Lymphohistiocytosis Associated with Natural T-cell Leukemia |
title_fullStr | Hemophagocytic Lymphohistiocytosis Associated with Natural T-cell Leukemia |
title_full_unstemmed | Hemophagocytic Lymphohistiocytosis Associated with Natural T-cell Leukemia |
title_short | Hemophagocytic Lymphohistiocytosis Associated with Natural T-cell Leukemia |
title_sort | hemophagocytic lymphohistiocytosis associated with natural t-cell leukemia |
topic | Pathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6476604/ https://www.ncbi.nlm.nih.gov/pubmed/31058001 http://dx.doi.org/10.7759/cureus.4107 |
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