Orbital Rosai–Dorfman Disease in a fifty-eight years old woman

Rosai–Dorfman disease (RDD) is rare and characterized by histiocytic proliferation and massive cervical lymphadenopathy. About 40% of patients have extra-nodal involvement. Opthalmic involvement is seen in 10% of cases. A case of orbital Rosai Dorfman disease in a 58 years old woman is presented her...

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Autores principales: Li, Hui-Yan, Cui, Hong-Guang, Zheng, Xue-Yong, Ren, Guo-Ping, Gu, Yang-Shun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publicaitons 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817788/
https://www.ncbi.nlm.nih.gov/pubmed/24353690
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author Li, Hui-Yan
Cui, Hong-Guang
Zheng, Xue-Yong
Ren, Guo-Ping
Gu, Yang-Shun
author_facet Li, Hui-Yan
Cui, Hong-Guang
Zheng, Xue-Yong
Ren, Guo-Ping
Gu, Yang-Shun
author_sort Li, Hui-Yan
collection PubMed
description Rosai–Dorfman disease (RDD) is rare and characterized by histiocytic proliferation and massive cervical lymphadenopathy. About 40% of patients have extra-nodal involvement. Opthalmic involvement is seen in 10% of cases. A case of orbital Rosai Dorfman disease in a 58 years old woman is presented here, who was misdiagnosed as orbital inflammatory disease initially. The patient did not respond to a course of oral prednisolone. Then complete surgical excision of the mass was performed and the histopathological examination was consistent with a diagnosis of RDD.
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spelling pubmed-38177882013-12-18 Orbital Rosai–Dorfman Disease in a fifty-eight years old woman Li, Hui-Yan Cui, Hong-Guang Zheng, Xue-Yong Ren, Guo-Ping Gu, Yang-Shun Pak J Med Sci Case Report Rosai–Dorfman disease (RDD) is rare and characterized by histiocytic proliferation and massive cervical lymphadenopathy. About 40% of patients have extra-nodal involvement. Opthalmic involvement is seen in 10% of cases. A case of orbital Rosai Dorfman disease in a 58 years old woman is presented here, who was misdiagnosed as orbital inflammatory disease initially. The patient did not respond to a course of oral prednisolone. Then complete surgical excision of the mass was performed and the histopathological examination was consistent with a diagnosis of RDD. Professional Medical Publicaitons 2013 /pmc/articles/PMC3817788/ /pubmed/24353690 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Li, Hui-Yan
Cui, Hong-Guang
Zheng, Xue-Yong
Ren, Guo-Ping
Gu, Yang-Shun
Orbital Rosai–Dorfman Disease in a fifty-eight years old woman
title Orbital Rosai–Dorfman Disease in a fifty-eight years old woman
title_full Orbital Rosai–Dorfman Disease in a fifty-eight years old woman
title_fullStr Orbital Rosai–Dorfman Disease in a fifty-eight years old woman
title_full_unstemmed Orbital Rosai–Dorfman Disease in a fifty-eight years old woman
title_short Orbital Rosai–Dorfman Disease in a fifty-eight years old woman
title_sort orbital rosai–dorfman disease in a fifty-eight years old woman
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817788/
https://www.ncbi.nlm.nih.gov/pubmed/24353690
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AT zhengxueyong orbitalrosaidorfmandiseaseinafiftyeightyearsoldwoman
AT renguoping orbitalrosaidorfmandiseaseinafiftyeightyearsoldwoman
AT guyangshun orbitalrosaidorfmandiseaseinafiftyeightyearsoldwoman

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