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.
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
Similar
MEDLINE
...
LILACS
LIS