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一例门克斯卷发综合征尸检病例。

An autopsy case of Menkes kinky hair disease.

作者信息

Matsubara O, Takaoka H, Nasu M, Iwakawa Y, Okeda R

出版信息

Acta Pathol Jpn. 1978 Jul;28(4):585-94. doi: 10.1111/j.1440-1827.1978.tb00897.x.

Abstract

An autopsy cases of Menkes kinky hair disease in a 1 year and 8 months old male infant is presented and compared with the morphological findings of the previous literatures. The main pathological changes are atrophy of the whole cerebellar cortex and bilateral temporal lobe, atrophy with demyelination of the white matter, tortuous running of the cerebral arteries, multiple diverticulosis of the urinary bladder and hyaline-like deposition in the gastric submucosa. Microscopically, the peculiar degenerative change of Purkinje cell (somal sprout) is the only characteristic lesion in our case and the others. It is suggested that Menkes kinky hair disease may be a syndrome due to metabolic disturbance appearing not only in ectoderm such as the central nervous system, but also in mesoderm such as connective tissue and bone.

摘要

本文报告了一例1岁8个月男婴的门克斯卷发综合征尸检病例,并与以往文献中的形态学发现进行了比较。主要病理变化为全小脑皮质和双侧颞叶萎缩、白质萎缩伴脱髓鞘、脑动脉迂曲走行、膀胱多发憩室形成以及胃黏膜下层透明样沉积。镜下,浦肯野细胞的特殊退行性改变(体细胞芽生)是本例及其他病例唯一的特征性病变。提示门克斯卷发综合征可能是一种由于代谢紊乱引起的综合征,不仅出现在外胚层,如中枢神经系统,也出现在中胚层,如结缔组织和骨骼。

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