Extranodal Rosai–Dorfman disease manifesting as Sjögren’s syndrome combined with panuveitis and hypertrophic pachymeningitis: a case report and review of literature

Extranodal Rosai–Dorfman disease manifesting as Sjögren’s syndrome combined with panuveitis and hypertrophic pachymeningitis: a case report and review of literature

Rosai–Dorfman disease (RDD) is a rare non-Langerhans cell histiocytosis characterized by massive lymphadenopathy and systemic extranodal lesions. We present the case of a 28-year-old woman who presented with recurrent blurred vision in her right eye for 3 months. She developed blindness and atrophy...

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Bibliographic Details
Main Authors: Jing Xu, Meihua Huang, Binsong Dong, Min Jian, Jinyu Chen, Naiyuan Zhang, Chunlian Ou, Yongming Wu, Dongmei Wang
Format: Article
Language:English
Published: SAGE Publishing 2024-04-01
Series:Journal of International Medical Research
Online Access:https://doi.org/10.1177/03000605241233141

Internet

https://doi.org/10.1177/03000605241233141

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