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[脊髓小脑变性的神经病理学背景——特别提及橄榄脑桥小脑萎缩、夏伊-德雷格综合征和多系统萎缩中的自主神经系统病变]

[Neuropathological background of spinocerebellar degeneration--with special reference to autonomic nervous system lesions in olivopontocerebellar atrophy, Shy-Drager syndrome and multiple system atrophy].

作者信息

Mizutani T

出版信息

No To Shinkei. 1985 Jul;37(7):675-85.

PMID:4063122
Abstract

For elucidation of actual status of olivopontocerebellar atrophy (OPCA) in nosological relation to Shy-Drager syndrome (SDS) and multiple system atrophy (MSA), neuropathological examination with morphometric survey on the intermediolateral column of the spinal cord was performed. The materials were 13 cases registered in our laboratory. Clinically, they consisted of 9 sporadic OPCA including 2 cases with prominent autonomic failure, and 4 hereditary spinocerebellar degeneration. In the autonomic nervous system of CNS, degeneration of the intermediolateral column was found in the sporadic cases without exception, irrespective of presence or absence of orthostatic hypotension, while the hereditary cases showed neither orthostatic hypotension nor neuronal loss in the nucleus. The autonomic centers in the brain-stem and cerebellum were systematically affected in both the sporadic and the hereditary cases. It was particularly remarked that the fastigial nucleus, tractus and nucleus solitarius, which have been suggested to be related to cardiovascular control, was severely affected. The locus coeruleus, on the other hand, was less severely affected in the hereditary cases. The most remarkable finding was that there was no case with neuropathological change restricted only to the olivo-ponto-cerebellar (OPC) and/or autonomic nervous systems. The sporadic cases had OPC system degeneration with striato-nigral degeneration (SND) and autonomic nervous system degenerations, irrespective of differences in clinical features from case to case. It should be emphasized that the actual neuropathological status of our sporadic cases could be regarded as a multisystemic degeneration inevitably combined with OPC system degeneration, apart from whether such cases are designated as MSA or not. Finally it was remarked that the hereditary cases were different from the sporadic cases in that there occurred far less severe involvement of the locus coeruleus and intermediolateral column, and primary degeneration of the substantia nigra different obviously from SND.

摘要

为阐明橄榄体脑桥小脑萎缩(OPCA)在病因学上与夏伊-德雷格综合征(SDS)和多系统萎缩(MSA)的实际关系,我们对脊髓中间外侧柱进行了形态计量学的神经病理学检查。材料为我们实验室登记的13例病例。临床上,包括9例散发性OPCA(其中2例有明显自主神经功能衰竭)和4例遗传性脊髓小脑变性。在中枢神经系统的自主神经系统中,散发性病例无一例外均发现中间外侧柱变性,无论是否存在体位性低血压,而遗传性病例既无体位性低血压,核内也无神经元丢失。脑干和小脑中的自主神经中枢在散发性和遗传性病例中均受到系统性影响。特别值得注意的是,已被认为与心血管控制有关的顶核、孤束核和束严重受累。另一方面,遗传性病例中蓝斑受累较轻。最显著的发现是,没有一例神经病理学改变仅局限于橄榄体脑桥小脑(OPC)和/或自主神经系统。散发性病例存在OPC系统变性伴纹状体黑质变性(SND)和自主神经系统变性,尽管各病例临床特征存在差异。应该强调的是,我们散发性病例的实际神经病理学状况可被视为不可避免地与OPC系统变性合并的多系统变性,无论这些病例是否被诊断为MSA。最后值得注意的是,遗传性病例与散发性病例的不同之处在于,蓝斑和中间外侧柱受累程度较轻,黑质原发性变性明显不同于SND。

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