Isolated intracranial Rosai-Dorfman disease mimicking suprasellar meningioma: case report with review of the literature.
作者： S Swan , X Teng , R Zhan , J Yu , J Gu
DOI: 10.1177/147323000803600535
关键词:
摘要: Rosai-Dorfman disease (RDD) is an idiopathic histiocytic proliferation affecting the lymph nodes. Isolated intracranial RDD rare and usually appears as a well-defined, dural-based lesion without lymphadenopathy. The clinical radiological features of are similar to meningioma. Histopathology immunohistochemistry essential for definitive diagnosis. This report 43-year old male with isolated RDD, which manifested suprasellar clinical, pathological aspects discussed within context review previously reported cases.
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