[Nuclear syndrome of the oculomotor nerve caused by a mesencephalic infarction confirmed by MRI].

Archivos de neurobiologia Pub Date : 1992-07-01
V Mateos, D M Campos, V P Colosía, J Salas-Puig, J M Fernández, C H Lahoz
{"title":"[Nuclear syndrome of the oculomotor nerve caused by a mesencephalic infarction confirmed by MRI].","authors":"V Mateos,&nbsp;D M Campos,&nbsp;V P Colosía,&nbsp;J Salas-Puig,&nbsp;J M Fernández,&nbsp;C H Lahoz","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The nuclear syndrome of the third nerve was first described in 1981. It has the very characteristic disturbance of an ophthalmoplegia with complete ipsilateral third nerve palsy associated with paresis of elevation in contralateral eye. This particularly presentation is due to the innervation of the superior rectus which comes mainly from the contralateral oculomotor nucleus. As associated signs were described contralateral cerebellar and or pyramidal syndromes, uni or bilateral parasympathetic disfunction and sometimes gaze disorders. The etiology es usually a vascular damage (ischemic most frequently) located in mesencephalon. We report on a case of a 60 years old man who developed acute nuclear ophthalmoplegia of the third right nerve accompanied with cerebellar and pyramidal syndrome and focal asterixis in left extremities. MRI showed an ischemic lesion in right paramedial mesencephalic territory with extension to the ipsilateral thalamic region. Pyramidal and cerebellar syndromes and asterixis disappeared in a few weeks, while ophthalmoplegia remained unchanged. Semiologic characteristics and anatomic basis of the nuclear oculomotor syndrome which allow to make the differential diagnosis between this syndrome and intra-axial fascicular disturbances of the third nerve (Weber, Claude and Benedikt syndromes) are discuss.</p>","PeriodicalId":8654,"journal":{"name":"Archivos de neurobiologia","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1992-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archivos de neurobiologia","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The nuclear syndrome of the third nerve was first described in 1981. It has the very characteristic disturbance of an ophthalmoplegia with complete ipsilateral third nerve palsy associated with paresis of elevation in contralateral eye. This particularly presentation is due to the innervation of the superior rectus which comes mainly from the contralateral oculomotor nucleus. As associated signs were described contralateral cerebellar and or pyramidal syndromes, uni or bilateral parasympathetic disfunction and sometimes gaze disorders. The etiology es usually a vascular damage (ischemic most frequently) located in mesencephalon. We report on a case of a 60 years old man who developed acute nuclear ophthalmoplegia of the third right nerve accompanied with cerebellar and pyramidal syndrome and focal asterixis in left extremities. MRI showed an ischemic lesion in right paramedial mesencephalic territory with extension to the ipsilateral thalamic region. Pyramidal and cerebellar syndromes and asterixis disappeared in a few weeks, while ophthalmoplegia remained unchanged. Semiologic characteristics and anatomic basis of the nuclear oculomotor syndrome which allow to make the differential diagnosis between this syndrome and intra-axial fascicular disturbances of the third nerve (Weber, Claude and Benedikt syndromes) are discuss.

[MRI证实中脑梗死所致动眼神经核综合征]。
第三神经核综合征于1981年首次报道。它具有非常特征性的眼麻痹与完全性同侧第三神经麻痹相关的对侧眼仰角轻瘫。这种特殊的表现是由于上直肌的神经支配主要来自对侧动眼肌核。相关症状包括对侧小脑和/或锥体综合征,单侧或双侧副交感神经功能障碍,有时还包括凝视障碍。病因通常是位于中脑的血管损伤(最常见的是缺血性)。我们报告了一个60岁的男子谁发展急性核性眼麻痹的第三神经右伴小脑和锥体综合征和局灶性星形肌在左肢体。MRI显示右侧副中脑区缺血性病变,并延伸至同侧丘脑区。锥体综合征和小脑综合征及星形肌在几周内消失,而眼麻痹没有变化。讨论了核动眼病综合征的符号学特征和解剖学基础,以便鉴别诊断该综合征与第三神经轴束内紊乱(Weber, Claude和Benedikt综合征)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信