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Isolated intracranial Rosai Dorfman disease masquerading as meningioma: a case report.

Nandita Ghosal,Ganesh Murthy,Visvanathan Krishnaswamy,Manthravadi Sridhar,A. S. Hegde-2007-04-01-PubMed
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TL;DRAbstract

Isolated intracranial Rosai Dorfman disease (sinus histiocytosis with massive lymphadenopathy) is rare. We present a 26-year-old male who presented with left focal motor seizures becoming secondarily generalized of one-year duration. Clinically and radiologically patient was diagnosed to have a right parietal convexity meningioma. However on histopathological examination a final diagnosis of intracranial Rosai Dorfman disease was rendered.

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Isolated intracranial Rosai Dorfman disease (sinus histiocytosis with massive lymphadenopathy) is rare. We present a 26-year-old male who presented with left focal motor seizures becoming secondarily generalized of one-year duration. Clinically and radiologically patient was diagnosed to have a right parietal convexity meningioma. However on histopathological examination a final diagnosis of intracranial Rosai Dorfman disease was rendered.

Keywords

Rosai–Dorfman diseaseMedicineMeningiomaSinus Histiocytosis with Massive LymphadenopathyHistopathological examinationHistiocytosisDiseaseSinus (botany)

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