Extranodal (dural) Rosai-Dorfman disease radiologically and histologically mimicking meningioma: a case report.

@article{Nassif2015ExtranodalR,
  title={Extranodal (dural) Rosai-Dorfman disease radiologically and histologically mimicking meningioma: a case report.},
  author={Samer Nassif and Fouad I Boulos},
  journal={Analytical and quantitative cytopathology and histopathology},
  year={2015},
  volume={37 2},
  pages={144-6}
}
BACKGROUND Rosai-Dorfman disease (sinus histiocytosis with massive lymphadenopathy) is an idiopathic nonneoplastic lymphohistiocytic proliferation with variable clinical presentations, sometimes mimicking other disorders including neoplasm. Particularly, intracranial Rosai-Dorfman disease is rare and without well-established optimal treatment modalities. CASE A 42-year-old man presented with gradually progressive unilateral hearing and vision loss over a two-year period. An MRI of the head… CONTINUE READING