Ghosal Nandita, Murthy Ganesh, Visvanathan K, Sridhar M, Hegde A S
Department of Pathology & Transfusion Medicine, Sri Sathya Sai Institute of Higher Medical Sciences, Bangalore.
Indian J Pathol Microbiol. 2007 Apr;50(2):382-4.
Isolated intracranial Rosai Dorfman disease (sinus histiocytosis with massive lymphadenopathy) is rare. We present a 26-year-old male who presented with left focal motor seizures becoming secondarily generalized of one-year duration. Clinically and radiologically patient was diagnosed to have a right parietal convexity meningioma. However on histopathological examination a final diagnosis of intracranial Rosai Dorfman disease was rendered.
孤立性颅内罗萨伊-多夫曼病（伴巨大淋巴结病的窦性组织细胞增多症）较为罕见。我们报告一名26岁男性，出现左侧局灶性运动性癫痫发作，继发全身性发作，病程1年。临床和影像学检查诊断该患者患有右顶叶凸面脑膜瘤。然而，经组织病理学检查，最终诊断为颅内罗萨伊-多夫曼病。
Zotero 插件