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[以脑缺血发作表现的科凯恩综合征:病例报告]

[Cockayne's syndrome presenting cerebral ischemic attack: case report].

作者信息

Shirasaki N, Hayashi M, Handa Y, Kabuto M, Tsuji T, Kawano H, Kobayashi H

出版信息

No To Shinkei. 1986 Sep;38(9):871-5.

PMID:3790368
Abstract

A 29-year-old man with Cockayne's syndrome (CS), presenting reversible ischemic neurological deficit is reported. In his past history, hearing disturbance developed at 6 years old and visual disturbance at 12 years old. His parents have consanguinious marriage. He came to our hospital complaining of right-sided hemiparesis and speech disturbance. He was 115.8 cm tall and his weight 20 kg. The characteristic manifestation of CS, i. e., dwarfism, mental retardadation, cachectic feature, retinal atrophy, neural deafness and calcification of bilateral basal ganglia were all noticed. A CT scan on admission revealed marked brain atrophy as well as the intracranial calcifications, while no lesions compatible with his neurological findings were detected. Cerebral ischemic state was mostly suspected. Following up with conservative therapy by the use of fibrinolytic agent, his neurological deteriorations disappeared on the 4th hospital day. Cerebral angiograms showed stenotic lesions of both C1-C2 portion of the left internal carotid artery and the right middle cerebral artery, and the aneurysm in the right internal carotid artery. Such atherosclerotic vascular change as observed in the cerebral angiograms in this case have progressed rapidly for his age. In this case, diabetes mellitus and hyperlipoproteinemia such as increased total cholesterol, increased triglyceride, decreased HDL and increased apoprotein B and C II were complicated for the risk factor of the atherosclerosis. It's controversial that early progress of atherosclerosis is due to ideopathic original feature of CS or to the secondary change from these complications.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

报告了一名患有科凯恩综合征(CS)的29岁男性,表现为可逆性缺血性神经功能缺损。他既往6岁时出现听力障碍,12岁时出现视力障碍。他的父母为近亲结婚。他因右侧偏瘫和言语障碍前来我院就诊。他身高115.8厘米,体重20千克。CS的典型表现,即侏儒症、智力发育迟缓、恶病质特征、视网膜萎缩、神经性耳聋和双侧基底节钙化均被发现。入院时的CT扫描显示明显的脑萎缩以及颅内钙化,然而未检测到与他的神经学表现相符的病变。最怀疑为脑缺血状态。在使用纤溶药物进行保守治疗后随访,他的神经功能恶化在住院第4天消失。脑血管造影显示左侧颈内动脉C1 - C2段和右侧大脑中动脉均有狭窄病变,以及右侧颈内动脉有动脉瘤。就他的年龄而言,本例脑血管造影中观察到的这种动脉粥样硬化血管改变进展迅速。在这种情况下,糖尿病和高脂血症,如总胆固醇升高、甘油三酯升高、高密度脂蛋白降低以及载脂蛋白B和C II升高,作为动脉粥样硬化的危险因素并发。动脉粥样硬化的早期进展是由于CS的特发性原始特征还是这些并发症的继发改变存在争议。(摘要截短至250字)

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