[Lhermitte-Duclos disease. Case report and review of the literature].

S Györi, P Molnár
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引用次数: 0

Abstract

A new case of Lhermitte-Duclos disease was recognized as an accidental finding during the autopsy of a 58-year-old male who had died because of acute enteritis and shock-induced cardiac failure. Gross examination revealed focally disturbed cerebellar cortical structure in two foci. Microscopical investigation resulted in findings typical of Lhermitte-Duclos disease: 1. Broadened molecular layer containing myelinated axonal projections; 2. Disappearance of Purkinje cells; 3. Progressive hypertrophy of the granular cells within the granular layer; 4. Loss of the central white matter core of the cerebellar folia. The etiology and pathogenesis of the lesion is still unclear. With this first report in Hungarian the authors wish to call the attention to this rare disease.

[Lhermitte-Duclos疾病。病例报告及文献回顾]。
一个新的病例Lhermitte-Duclos病被认为是一个意外的发现在尸检58岁的男性谁死于急性肠炎和休克引起的心力衰竭。大体检查显示两个病灶的小脑皮质结构局部紊乱。显微镜检查结果显示典型的Lhermitte-Duclos病:加宽的分子层包含髓鞘轴突;2. 浦肯野细胞消失;3.颗粒层内颗粒细胞进行性肥大;4. 小脑叶中央白质核心的缺失。该病变的病因和发病机制尚不清楚。这是匈牙利语的第一份报告,作者希望引起人们对这一罕见疾病的注意。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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