Kim M, Provias J, Bernstein M
Department of Pathology, Toronto Hospital, University of Toronto, Ontario, Canada.
Neurosurgery. 1995 Jun;36(6):1185-7. doi: 10.1227/00006123-199506000-00019.
Rosai-Dorfman disease is a rare idiopathic histioproliferative disease affecting the lymph nodes. Extranodal involvement has also been recognized, but central nervous system manifestations are extremely rare. Only 12 patients with intracranial involvement have been reported previously, and they all presented with clinical and radiological findings suggestive of meningioma. We report multiple meningeal nodules in a patient presenting with seizures whose pathological findings at surgery confirmed the diagnosis of Rosai-Dorfman disease. A review of all previously reported intracranial lesions is presented.
罗萨伊-多夫曼病是一种罕见的特发性组织细胞增生性疾病,累及淋巴结。结外受累也已得到确认,但中枢神经系统表现极为罕见。此前仅报道过12例颅内受累患者,他们均表现出提示脑膜瘤的临床和影像学表现。我们报告了1例以癫痫发作为表现的患者,其手术病理结果证实为罗萨伊-多夫曼病,该患者存在多个脑膜结节。本文对所有先前报道的颅内病变进行了综述。