Meningeal Rosai-Dorfman Disease Presenting as an Intracranial Mass – Report of a Case with Review of the Literature

Author:

Pattnaik Niharika1,Parmar Rajni2,Nayak Biswaranjan3,Sampat Nakul Y.1,Jha Shilpy1,Jena Manas R.4,Barik Lalit M.1,Mishra Sourav K.5,Munjal Gauri1,Chottaraji Anirudha6,Mohanty Sambit K.1ORCID

Affiliation:

1. Department of Pathology and Laboratory Medicine, Advanced Medical Research Institute, Bhubaneswar, India

2. Department of Pathology and laboratory Medicine, The Lal Pathology Laboratories, Delhi, India

3. Department of Neurosurgery, Advanced Medical Research Institute, Bhubaneswar, India

4. Department of Radiology, Advanced Medical Research Institute, Bhubaneswar, India

5. Department of Medical Oncology, Advanced Medical Research Institute, Bhubaneswar, India

6. Department of Pathology, Oncquest Laboratories, Delhi, India

Abstract

Meningeal Rosai-Dorfman disease, a type of sporadic Rosai-Dorfman disease, is a rare occurrence. A few cases are reported in the English literature with an adequate immunohistochemical workup. This entity clinically and radiologically mimics either a meningeal or a parenchymal neoplasm with meningeal extension, warranting a thorough histopathologic evaluation. A broad histologic differential necessitates a detailed immunohistochemical characterization to render a correct diagnosis that has significant therapeutic and prognostic implications. Herein, we report a case of isolated meningeal Rosai-Dorfman disease in a 50-years-old human immunodeficiency virus-positive male patient with an emphasis on the histopathology, immunoprofile, and differential diagnoses.

Publisher

SAGE Publications

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

Reference22 articles.

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