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多系统萎缩中神经元胞质内包涵体的分布

Distribution of neuronal cytoplasmic inclusions in multiple system atrophy.

作者信息

Sugiura K, Hashizume Y, Kume A, Takahashi A

机构信息

Department of Neurology, Nagoya University School of Medicine, Japan.

出版信息

Nagoya J Med Sci. 1995 Dec;58(3-4):117-26.

PMID:8725495
Abstract

Neuronal cytoplasmic inclusions (NCIs) were demonstrated by means of silver staining (Gallyas staining) in the central nervous systems of 18 deceased patients with multiple system atrophy (MSA) - 6 with olivopontocerebellar atrophy (OPCA), 6 with striatonigral degeneration (SND) and 6 with Shy-Drager syndrome (SDS). We observed NCIs in the cerebral cortex, putamen, pons, medulla oblongata and spinal cord, and especially in the putamen and pons of all cases with MSA. No NCIs were observed in the cerebellum and midbrain. The findings were common to all 3 subtypes of MSA. NCIs were not present in patients with other neurodegenerative disorders and non-neurological disorders. Our findings indicate that NCIs represent a special neuronal alteration characteristic of MSA and support the theory that OPCA, SND and SDS represent manifestations of a single condition i.e. MSA.

摘要

通过银染法(加利亚斯染色)在18例已故多系统萎缩(MSA)患者的中枢神经系统中证实了神经元胞质包涵体(NCI)——其中6例为橄榄脑桥小脑萎缩(OPCA),6例为纹状体黑质变性(SND),6例为夏伊-德雷格综合征(SDS)。我们在大脑皮质、壳核、脑桥、延髓和脊髓中观察到了NCI,尤其是在所有MSA病例的壳核和脑桥中。在小脑和中脑中未观察到NCI。这些发现是MSA所有3个亚型共有的。在其他神经退行性疾病和非神经疾病患者中未发现NCI。我们的发现表明,NCI代表MSA特有的一种特殊神经元改变,并支持OPCA、SND和SDS代表单一疾病即MSA的不同表现形式这一理论。

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