Neuropathology of various types of Niemann-Pick disease.

M Elleder, A Jirásek
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引用次数: 27

Abstract

A comparative neuropathological and histochemical study was performed on the brains of seven cases of NPD. In type A (two cases), besides the neuronal storage of SM, a widespread endothelial storage of a neutral glycosphingolipid was found. In one case a pseudosystemic lesion of the pallido-nigral system was observed. In type B (one case) the only finding was the endothelial storage of SM. In type C (four cases) the degree of neuronal storage distension contrasted considerably with a very low amount of lipid demonstrable histochemically in fixed brains. Only in one case, focal neuronal storage of a phosphoglyceride could be proved. However, in peripheral neurons (of unfixed appendix) the phosphoglycerides were clearly predominating (one case). A remarkable and constant finding in each case of the series was a widespread neuroaxonal dystrophy with various topical maxima (thalamus, dentate nuclei). The significance of the findings are discussed in relation to the present status of knowledge of this type.

不同类型尼曼-匹克病的神经病理学。
对7例NPD患者的大脑进行了比较神经病理和组织化学研究。在A型(2例)中,除了SM的神经元储存外,还发现了广泛的中性鞘糖脂内皮储存。在一个情况下,假性全身病变的苍白神经系统被观察到。在B型(1例)中,唯一的发现是SM的内皮储存。在C型(4例)中,神经元储存扩张的程度与固定脑中非常低的脂质含量形成了相当大的对比。只有在一个案例中,可以证明局部神经元储存磷酸甘油酯。然而,在周围神经元(未固定阑尾)中,甘油三酯明显占优势(1例)。在该系列的每个病例中,一个显著且持续的发现是广泛的神经轴突营养不良,具有各种局部最大值(丘脑,齿状核)。研究结果的意义,讨论了有关这类知识的现状。
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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