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脉络丛血管瘤伴面部葡萄酒色斑:与斯特奇-韦伯综合征的关系——病例报告

Choroid plexus hemangioma with port-wine nevus of the face: relationship to Sturge-Weber syndrome--case report.

作者信息

Kato K, Banno M, Kanzaki M

机构信息

Department of Neurosurgery, Kamo Hospital, Aichi.

出版信息

Neurol Med Chir (Tokyo). 1990 Sep;30(9):703-6. doi: 10.2176/nmc.30.703.

Abstract

The authors describe a case of choroid plexus hemangioma in a 49-year-old male. Computed tomographic scan showed an isodense mass at the trigone of the right lateral ventricle with homogeneous enhancement. He also displayed a port-wine nevus on the ipsilateral side of the face. At operation, the tumor was found not to adhere to the lateral ventricular wall but to be connected to the choroid plexus, and was colored similarly to the facial nevus. Histological examination showed a capillary hemangioma with many crowded capillaries. This case was not included in the category of Sturge-Weber syndrome but is thought to be closely related, considering the syndrome from the viewpoint of generalized neurocutaneous hemangiomatosis.

摘要

作者描述了一例49岁男性脉络丛血管瘤病例。计算机断层扫描显示右侧侧脑室三角区有一等密度肿块,强化均匀。他同侧面部还有葡萄酒色斑痣。手术中发现肿瘤未附着于侧脑室壁,而是与脉络丛相连,且颜色与面部痣相似。组织学检查显示为毛细血管瘤,有许多密集的毛细血管。该病例不属于斯特奇-韦伯综合征范畴,但从广义神经皮肤血管瘤病角度考虑该综合征,认为两者密切相关。

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