Isolated Intracranial Rosai-Dorfman Disease Mimicking Suprasellar Meningioma: Case Report with Review of the Literature
2008 ◽
Vol 36
(5)
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pp. 1134-1139
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Keyword(s):
Rosai-Dorfman disease (RDD) is an idiopathic histiocytic proliferation affecting the lymph nodes. Isolated intracranial RDD is rare and usually appears as a well-defined, dural-based lesion without lymphadenopathy. The clinical and radiological features of intracranial RDD are similar to meningioma. Histopathology and immunohistochemistry are essential for a definitive diagnosis. This is a report of a 43-year old male with isolated intracranial RDD, which manifested as a suprasellar meningioma. The clinical, radiological and pathological aspects of the disease are discussed within the context of a review of previously reported cases.
Keyword(s):
2013 ◽
Vol 33
(2)
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pp. 120-123
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Keyword(s):
2012 ◽
Vol 3
(7)
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pp. 340-342
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Keyword(s):
2012 ◽
Vol 8
(4)
◽
pp. 647
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1999 ◽
Vol 91
(2)
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pp. 335-339
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2009 ◽
Vol 20
(1)
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pp. 59-65
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2003 ◽
Vol 35
(2)
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pp. 165-167
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2003 ◽
Vol 127
(3)
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pp. e139-e141
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