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[1例伴有双侧大脑中动脉闭塞及烟雾病样现象的普拉德-威利综合征]

[A case of Prader-Willi syndrome with bilateral middle cerebral artery occlusion and moyamoya phenomenon].

作者信息

Kusuhara T, Ayabe M, Hino H, Shoji H, Neshige R

机构信息

First Department (Neurology) of Internal Medicine, Kurume University, School of Medicine.

出版信息

Rinsho Shinkeigaku. 1996 Jun;36(6):770-3.

PMID:8937199
Abstract

We report a case of Prader-Willi syndrome (PWS) complicated with juvenile stroke. The patient is a 19-year-old man with right hemiplegia, who has had a history of non-insulin-dependent diabetes mellitus (NIDDM) for ten years. The diagnosis of PWS was confirmed genetically by the method of fluorescence in situ hybridization which showed the deletion of chromosome 15. His brain MRI revealed abnormal signal intensities in the left basal ganglia and around the right trigone of the lateral ventricle. Angiographic examination showed occlusions of bilateral proximal middle cerebral arteries with basal moyamoya vessels. The left vertebral artery was also occluded at its origin. Only a few cases of PWS complicated with stroke have been reported before and, to date, there has been no case with arterial occlusion similar to our case. Though the cause of these arterial occlusions is unknown, it may be related to arteriosclerosis following NIDDM.

摘要

我们报告一例普拉德-威利综合征(PWS)合并青少年卒中的病例。患者为一名19岁男性,有右侧偏瘫,患非胰岛素依赖型糖尿病(NIDDM)已有十年病史。通过荧光原位杂交方法进行基因检测确诊为PWS,结果显示15号染色体缺失。他的脑部MRI显示左侧基底神经节及右侧侧脑室三角区周围信号强度异常。血管造影检查显示双侧大脑中动脉近端闭塞,伴有基底烟雾状血管形成。左侧椎动脉起始部也闭塞。此前仅有少数PWS合并卒中的病例报道,迄今为止,尚无与我们病例类似的动脉闭塞情况。尽管这些动脉闭塞的原因尚不清楚,但可能与NIDDM后的动脉硬化有关。

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