Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Arun Kumar, Yadav, Yi Peng, Peng, Chen Chen, Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
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
_version_ 1782308859214299136
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