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伴室管膜瘤样分化的von Hippel-Lindau综合征1例 被引量:2

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摘要 目的分析von Hippel-Lindau(VHL)综合征的临床特征及病理特点。方法回顾性分析1例VHL综合征病人的临床资料,分析中枢神经系统血管母细胞瘤(HB)的影像学特点、病理特征及治疗。结果经乙状窦后入路手术全切除肿瘤,病理证实为伴胶质分化的HB。术后3个月MRI未见明显异常,病人一般状况良好。结论伴室管膜瘤分化的VHL综合征极为罕见,询问家族史、基因筛查有助于家族性VHL综合征的诊断及治疗。
出处 《中国微侵袭神经外科杂志》 CAS 2017年第12期567-568,共2页 Chinese Journal of Minimally Invasive Neurosurgery
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