Bilateral clinoidal Rosai Dorfman disease mimicking meningioma – a rare cause of bilateral blindness

Hrushikesh Kharosekar, Mayuresh Hinduja, Vernon Velho, Laxmikant Bhople
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Abstract

Rosai Dorfman disease is a self-limiting disease usually affecting the lymph nodes. Intracranial lesions are seen in less than 5% of cases. Isolated intracranial RDD without nodal involvement is rare, only 70 cases have been reported to date. Skull base lesions are seen in only 7 cases, petro clival RDD. Clionoidal lesions of RDD have not been reported in the literature, we report a rare case of bilateral Clionoidal lesions of RDD presenting with bilateral blindness in a young male.
模拟脑膜瘤的双侧斜面Rosai Dorfman病-一种罕见的双侧失明原因
罗赛多尔夫曼病是一种自限性疾病,通常影响淋巴结。颅内病变在不到5%的病例中可见。不累及淋巴结的孤立性颅内RDD是罕见的,迄今为止仅报道了70例。颅底病变仅7例见,斜坡性RDD。RDD的阴囊样体病变尚未在文献中报道,我们报告一例罕见的双侧阴囊样体病变的RDD表现为双侧失明的年轻男性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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