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橄榄体脑桥小脑萎缩中眼球运动障碍的神经病理学背景,特别提及缓慢扫视运动

Neuropathological background of oculomotor disturbances in olivopontocerebellar atrophy with special reference to slow saccade.

作者信息

Mizutani T, Satoh J, Morimatsu Y

机构信息

Department of Clinical Neuropathology, Tokyo Metropolitan Institute for Neurosciences, Japan.

出版信息

Clin Neuropathol. 1988 Mar-Apr;7(2):53-61.

PMID:3164663
Abstract

Neuropathological findings responsible for abnormal eye movements in olivopontocerebellar atrophy (OPCA) are reported. The material consists of eight sporadic cases and two hereditary cases. The sporadic cases showed impaired smooth pursuit without exception. The hereditary cases showed slow saccade (slow eye movement). Two important neuropathological findings are noted: The first is a systemic degeneration of cerebellifugal oculomotor control (cerebello-fastigio-vestibulo-MLF (medial longitudinal fasiculus) and perihypoglossal nuclei) in both types. Furthermore, neuronal loss of the oculomotor nuclei (oculomotor, trochlear and abducens nuclei) was found only in the hereditary cases. The second is that the hereditary type had a combined degeneration of the zona reticulata of the substantia nigra, the superior colliculus and the pontomedullary reticular formation. A review of the literature showed that all the cases of spino-cerebellar degeneration with slow saccade were hereditary OPCA, and that almost all cases had primary nigral degeneration. The neuropathological background of the oculomotor disturbances in OPCA is discussed.

摘要

本文报告了橄榄体脑桥小脑萎缩(OPCA)中导致眼球运动异常的神经病理学发现。材料包括8例散发性病例和2例遗传性病例。散发性病例无一例外均表现为平稳跟踪受损。遗传性病例表现为扫视缓慢(眼球运动缓慢)。有两个重要的神经病理学发现:第一个是两种类型中均存在小脑传出性眼球运动控制的系统性退化(小脑-顶核-前庭-内侧纵束(MLF)和舌下神经周核)。此外,仅在遗传性病例中发现动眼神经核(动眼神经、滑车神经和展神经核)的神经元丢失。第二个是遗传性类型存在黑质网状带、上丘和脑桥延髓网状结构的联合退化。文献回顾表明,所有伴有缓慢扫视的脊髓小脑变性病例均为遗传性OPCA,且几乎所有病例均有原发性黑质变性。本文讨论了OPCA中眼球运动障碍的神经病理学背景。

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