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Rosai-Dorfman Disease Complicated by Autoimmune Hemolytic Anemia in a Child: A Case Report and Review of the Literature
Rosai-Dorfman disease is a rare histiocytic proliferative disorder that commonly presents with a massive lymphadenopathy and a variety of constitutional symptoms. Severe hemolytic anemia is an infrequent complication of this disease. Although the etiology of the condition is unknown, infectious agen...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836236/ https://www.ncbi.nlm.nih.gov/pubmed/29515411 http://dx.doi.org/10.1159/000485968 |
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author | Lardhi, Amer A. Al-Mutairi, Abdullah K. Al-Qahtani, Mohammed H. Al-Mutairi, Atheer K. |
author_facet | Lardhi, Amer A. Al-Mutairi, Abdullah K. Al-Qahtani, Mohammed H. Al-Mutairi, Atheer K. |
author_sort | Lardhi, Amer A. |
collection | PubMed |
description | Rosai-Dorfman disease is a rare histiocytic proliferative disorder that commonly presents with a massive lymphadenopathy and a variety of constitutional symptoms. Severe hemolytic anemia is an infrequent complication of this disease. Although the etiology of the condition is unknown, infectious agents including viruses have been implicated. We describe a 2-year-old female child who presented with fever, pallor, and generalized lymphadenopathy complicated by the development of autoimmune hemolytic anemia. A review of the literature of this condition is also provided. |
format | Online Article Text |
id | pubmed-5836236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-58362362018-03-07 Rosai-Dorfman Disease Complicated by Autoimmune Hemolytic Anemia in a Child: A Case Report and Review of the Literature Lardhi, Amer A. Al-Mutairi, Abdullah K. Al-Qahtani, Mohammed H. Al-Mutairi, Atheer K. Case Rep Oncol Case Report Rosai-Dorfman disease is a rare histiocytic proliferative disorder that commonly presents with a massive lymphadenopathy and a variety of constitutional symptoms. Severe hemolytic anemia is an infrequent complication of this disease. Although the etiology of the condition is unknown, infectious agents including viruses have been implicated. We describe a 2-year-old female child who presented with fever, pallor, and generalized lymphadenopathy complicated by the development of autoimmune hemolytic anemia. A review of the literature of this condition is also provided. S. Karger AG 2018-01-19 /pmc/articles/PMC5836236/ /pubmed/29515411 http://dx.doi.org/10.1159/000485968 Text en Copyright © 2018 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Case Report Lardhi, Amer A. Al-Mutairi, Abdullah K. Al-Qahtani, Mohammed H. Al-Mutairi, Atheer K. Rosai-Dorfman Disease Complicated by Autoimmune Hemolytic Anemia in a Child: A Case Report and Review of the Literature |
title | Rosai-Dorfman Disease Complicated by Autoimmune Hemolytic Anemia in a Child: A Case Report and Review of the Literature |
title_full | Rosai-Dorfman Disease Complicated by Autoimmune Hemolytic Anemia in a Child: A Case Report and Review of the Literature |
title_fullStr | Rosai-Dorfman Disease Complicated by Autoimmune Hemolytic Anemia in a Child: A Case Report and Review of the Literature |
title_full_unstemmed | Rosai-Dorfman Disease Complicated by Autoimmune Hemolytic Anemia in a Child: A Case Report and Review of the Literature |
title_short | Rosai-Dorfman Disease Complicated by Autoimmune Hemolytic Anemia in a Child: A Case Report and Review of the Literature |
title_sort | rosai-dorfman disease complicated by autoimmune hemolytic anemia in a child: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836236/ https://www.ncbi.nlm.nih.gov/pubmed/29515411 http://dx.doi.org/10.1159/000485968 |
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