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Intracranial Rosai-Dorfman Disease
Rosai-Dorfman disease (RDD) is a rare, benign pseudolymphomatous condition, predominantly involving lymph nodes. Rosai-Dorfman disease (RDD) (sinus histiocytes with massive lymphadenopathy) rarely affects the intracranial region without involvement of other sites. It is a rare and idiopathic histopr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965928/ https://www.ncbi.nlm.nih.gov/pubmed/24707426 http://dx.doi.org/10.1155/2014/724379 |
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author | Arun Kumar, Yadav Yi Peng, Peng Chen Chen, Xia |
author_facet | Arun Kumar, Yadav Yi Peng, Peng Chen Chen, Xia |
author_sort | Arun Kumar, Yadav |
collection | PubMed |
description | Rosai-Dorfman disease (RDD) is a rare, benign pseudolymphomatous condition, predominantly involving lymph nodes. Rosai-Dorfman disease (RDD) (sinus histiocytes with massive lymphadenopathy) rarely affects the intracranial region without involvement of other sites. It is a rare and idiopathic histoproliferation disorder characterized by painless lymphadenopathy. We report a case of 43-year-old male who presented with unconsciousness; MRI was done and right temporofrontal mass was found. Excision was done, and on histopathology it confirmed RDD. |
format | Online Article Text |
id | pubmed-3965928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-39659282014-04-06 Intracranial Rosai-Dorfman Disease Arun Kumar, Yadav Yi Peng, Peng Chen Chen, Xia Case Rep Radiol Case Report Rosai-Dorfman disease (RDD) is a rare, benign pseudolymphomatous condition, predominantly involving lymph nodes. Rosai-Dorfman disease (RDD) (sinus histiocytes with massive lymphadenopathy) rarely affects the intracranial region without involvement of other sites. It is a rare and idiopathic histoproliferation disorder characterized by painless lymphadenopathy. We report a case of 43-year-old male who presented with unconsciousness; MRI was done and right temporofrontal mass was found. Excision was done, and on histopathology it confirmed RDD. Hindawi Publishing Corporation 2014 2014-02-11 /pmc/articles/PMC3965928/ /pubmed/24707426 http://dx.doi.org/10.1155/2014/724379 Text en Copyright © 2014 Yadav Arun Kumar 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 Arun Kumar, Yadav Yi Peng, Peng Chen Chen, Xia Intracranial Rosai-Dorfman Disease |
title | Intracranial Rosai-Dorfman Disease |
title_full | Intracranial Rosai-Dorfman Disease |
title_fullStr | Intracranial Rosai-Dorfman Disease |
title_full_unstemmed | Intracranial Rosai-Dorfman Disease |
title_short | Intracranial Rosai-Dorfman Disease |
title_sort | intracranial rosai-dorfman disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965928/ https://www.ncbi.nlm.nih.gov/pubmed/24707426 http://dx.doi.org/10.1155/2014/724379 |
work_keys_str_mv | AT arunkumaryadav intracranialrosaidorfmandisease AT yipengpeng intracranialrosaidorfmandisease AT chenchenxia intracranialrosaidorfmandisease |