Robain O, Aubourg P, Routon M C, Dulac O, Ponsot G
INSERM U-29, Paris, France.
Clin Neuropathol. 1988 Mar-Apr;7(2):47-52.
A neuropathological study of a case of Menkes disease is reported, illustrating the involvement of different types of neuronal cells. The cerebellum showed the most striking abnormalities: severe lack of internal granule cells. Purkinje cells with weeping willow pattern, numerous segmental enlargements of dendritic trunks and secondary branches, and presence of numerous eosinphilic spherical bodies in the molecular layer were the most conspicuous features. Using electron microscopy, the dendritic enlargements were observed to be made of both proliferated and enlarged mitochondria, and of saccules of smooth endoplasmic reticulum. The spheroid bodies in the molecular layer were mainly made of concentric lamellar structures which seemed to be proliferated smooth endoplasmic reticulum. The relationship between these morphological abnormalities and the metabolic disorder of Menkes disease is discussed.
本文报道了一例门克斯病的神经病理学研究,阐明了不同类型神经元细胞所受的影响。小脑表现出最显著的异常:内颗粒细胞严重缺乏。具有垂柳样形态的浦肯野细胞、树突主干和二级分支大量节段性增粗,以及分子层中存在大量嗜酸性球状体是最明显的特征。通过电子显微镜观察发现,树突增粗由增殖和增大的线粒体以及滑面内质网囊泡组成。分子层中的球状体主要由同心层状结构组成,似乎是增殖的滑面内质网。本文还讨论了这些形态学异常与门克斯病代谢紊乱之间的关系。