Intracranial Rosai-Dorfman Disease | Zendy

Yadav Arun Kumar | Zendy; Peng Yi Peng | Zendy; Xia Chen Chen | Zendy

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Intracranial Rosai-Dorfman Disease

Author(s) -

Yadav Arun Kumar,

Peng Yi Peng,

Xia Chen Chen

Publication year - 2014

Publication title -

case reports in radiology

Language(s) - English

Resource type - Journals

eISSN - 2090-6862

pISSN - 2090-6870

DOI - 10.1155/2014/724379

Subject(s) - rosai–dorfman disease , medicine , unconsciousness , histiocyte , emperipolesis , histopathology , pathology , cervical lymphadenopathy , lymph , sinus (botany) , disease , sinus histiocytosis with massive lymphadenopathy , dermatology , botany , psychiatry , biology , genus

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.

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