Suppr超能文献

青年成人慢性进行性白质脑病伴系统性动脉硬化

Chronic progressive leukoencephalopathy with systemic arteriosclerosis in young adults.

作者信息

Yokoi S, Nakayama H

出版信息

Clin Neuropathol. 1985 Jul-Aug;4(4):165-73.

PMID:4053457
Abstract

Clinicopathological studies of four cases of chronic progressive leukoencephalopathy with systemic arteriosclerosis are reported. Two patients were siblings. In all of our patients, the illness began in early adulthood (25-29 years of age), with gait and speech disturbance as the first symptoms. At about the same time, the patients complained of lumbago, caused by intervertebral disc hernia, and had a tendency toward baldness. They gradually developed disturbance of memory, dementia, spastic paraplegia, and positive pathological reflexes. After a few years, they could neither stand nor walk and became decerebrate. Blood pressures ranged from 120/60 to 140/80 mm Hg. Laboratory data were within normal limits, including serum cholesterol. EEG showed a generalized slowing. The illness ended in death after 9 years in one case and 3-4 years in the other three cases. A general autopsy was done in three cases and only the brain was autopsied in one case. The visceral organs and the brains were fixed in 10% formalin for macroscopic and histological studies. The general autopsies revealed arteriosclerosis in the small arteries of the heart, spleen, and kidneys in three cases and in addition, moderate arteriosclerosis of the coronary arteries in one. Remarkably uniform changes were found in the brains of all four cases, involving diffuse demyelination of the cerebral white matter, with some preservation of U-fibers, and small cystic and softening foci in the white matter and the basal ganglia. The cytoarchitecture of the cerebral cortex was well-preserved. The degeneration of the white matter was caused by arteriosclerotic changes of the small arteries: fibrous intimal proliferation and hyaline degeneration and splitting of the internal elastic membrane.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

报告了4例伴有系统性动脉硬化的慢性进行性白质脑病的临床病理研究。其中2例患者为兄弟姐妹。我们所有患者的疾病均始于成年早期(25 - 29岁),首发症状为步态和言语障碍。大约在同一时间,患者因椎间盘突出症抱怨腰痛,并有秃顶倾向。他们逐渐出现记忆障碍、痴呆、痉挛性截瘫及病理反射阳性。几年后,他们既不能站立也不能行走,呈去大脑状态。血压范围为120/60至140/80 mmHg。实验室检查数据包括血清胆固醇均在正常范围内。脑电图显示普遍性减慢。1例患者病程9年后死亡,另外3例患者病程3 - 4年后死亡。3例行全面尸检,1例仅对脑进行尸检。内脏器官和脑用10%福尔马林固定,用于宏观和组织学研究。全面尸检发现3例患者心脏、脾脏和肾脏的小动脉有动脉硬化,另外1例患者冠状动脉有中度动脉硬化。所有4例患者的脑均发现显著一致的改变,包括大脑白质弥漫性脱髓鞘,U形纤维部分保留,白质和基底节有小囊性软化灶。大脑皮质的细胞结构保存完好。白质变性是由小动脉的动脉硬化改变所致:纤维性内膜增生、透明变性及内弹性膜分裂。(摘要截取自250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验