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Isolated intracranial Rosai Dorfman disease masquerading as meningioma: a case report.
Indian J Pathol Microbiol ; 2007 Apr; 50(2): 382-4
Article in English | IMSEAR | ID: sea-72776
ABSTRACT
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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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Parietal Lobe / Brain Diseases / Humans / Male / Antigens, Differentiation, Myelomonocytic / S100 Proteins / Antigens, CD / Histiocytosis, Sinus / Adult / Diagnosis, Differential Type of study: Diagnostic study Language: English Journal: Indian J Pathol Microbiol Year: 2007 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Parietal Lobe / Brain Diseases / Humans / Male / Antigens, Differentiation, Myelomonocytic / S100 Proteins / Antigens, CD / Histiocytosis, Sinus / Adult / Diagnosis, Differential Type of study: Diagnostic study Language: English Journal: Indian J Pathol Microbiol Year: 2007 Type: Article