Spokes E G, Bannister R, Oppenheimer D R
J Neurol Sci. 1979 Sep;43(1):59-82. doi: 10.1016/0022-510x(79)90073-x.
Four cases of progressive autonomic failure are described, in all of which there were additional non-autonomic neurological abnormalities, including pyramidal, extra-pyramidal and cerebellar features. Histological examination revealed cell degeneration in the substantia nigra, putamen and intermediolateral columns of the spinal cord as a common pathological finding. In addition, 3 cases showed loss of Purkinje cells in the cerebellum and degeneration of pontine nuclei and inferior olivary nuclei. In one case there was cell loss from the locus coeruleus, caudate nucleus, vestibular nuclei and dorsal vagal nuclei. These were, therefore, cases of multiple system atrophy. Neurochemically, a common feature was a profound depletion in dopamine and noradrenaline from brain regions which are normally rich in these catecholamines. Central cholinergic systems appeared to be involved also, but to a variable degree.
本文描述了4例进行性自主神经功能衰竭病例,所有病例均伴有其他非自主神经的神经学异常,包括锥体束、锥体外系和小脑特征。组织学检查发现,黑质、壳核和脊髓中间外侧柱细胞变性是常见的病理表现。此外,3例患者小脑浦肯野细胞丢失,脑桥核和下橄榄核变性。1例患者蓝斑、尾状核、前庭核和迷走神经背核细胞丢失。因此,这些是多系统萎缩病例。神经化学方面,一个共同特征是通常富含这些儿茶酚胺的脑区中多巴胺和去甲肾上腺素显著减少。中枢胆碱能系统似乎也受到影响,但程度不一。