Isolated Intracranial Rosai-Dorfman Disease Mimicking Suprasellar Meningioma: Case Report with Review of the Literature
نویسندگان
چکیده
منابع مشابه
Isolated intracranial Rosai-Dorfman disease mimicking suprasellar meningioma: case report with review of the literature.
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 repo...
متن کاملIsolated intracranial Rosai-Dorfman disease mimicking meningioma.
Sinus histiocytosis with massive lymphadenopathy (SHML), also known as Rosai-Dorfman disease (RDD), is an idiopathic histiocytic proliferation affecting lymph nodes. It is typically characterized by painless cervical lymphadenopathy, fever and weight loss. Although extranodal involvement has been reported in diverse sites, intracranial presentation, particularly in the absence of nodal disease ...
متن کاملIsolated Intracranial Rosai-Dorfman Disease Mimicking Convexity Meningioma: A Case Report
Intracranial Rosai-Dorfman disease without systemic involvement is extremely rare. A 59-year-old woman presented with headaches. Magnetic resonance imaging revealed an enhancing posterior fossa convexity lesion with the dural tail sign. The preoperative diagnosis was meningioma. The histopathological examination revealed reactivity for S-100 and CD68 and non-reactivity for CD1a with emperipoles...
متن کاملRosai-Dorfman Disease: A Case Report and Literature Review
Rosai-Dorfman disease or sinus histiocytosis with massive lymphadenopathy is a rare disorder that typically manifests as lymphadenopathy and systemic symptoms whose etiology remains poorly elucidated. The diagnosis is based on immunohistochemistry. Its treatment is poorly defined but the prognosis is usually favorable. Here we report a 14 year old boy who presented with massive bilateral cervi...
متن کاملIsolated Intracranial Rosai-Dorfman Disease
Background. Rosai-Dorfman disease (RDD) is a benign histiocytic proliferative disorder of unknown etiology. This rare condition commonly causes massive cervical lymphadenopathy. Intracranial RDD without any nodal involvement is extremely rare. Case Report. A young Bangladeshi male complained of bilateral complete blindness with left sided deafness for about three years. There was no lymphadenop...
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ژورنال
عنوان ژورنال: Journal of International Medical Research
سال: 2008
ISSN: 0300-0605,1473-2300
DOI: 10.1177/147323000803600535