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《眼球运动中枢障碍:临床与局部解剖诊断、综合征及潜在疾病》

Central Ocular Motor Disorders: Clinical and Topographic Anatomical Diagnosis, Syndromes and Underlying Diseases.

机构信息

Neurologische Klinik der Ludwig-Maximilians-Universität München, Deutschland.

Deutsches Schwindel- und Gleichgewichtszentrum der Ludwig-Maximilians-Universität München, Deutschland.

出版信息

Klin Monbl Augenheilkd. 2021 Nov;238(11):1197-1211. doi: 10.1055/a-1654-0632. Epub 2021 Nov 16.

Abstract

The key to the diagnosis of ocular motor disorders is a systematic clinical examination of the different types of eye movements, including eye position, spontaneous nystagmus, range of eye movements, smooth pursuit, saccades, gaze-holding function, vergence, optokinetic nystagmus, as well as testing of the function of the vestibulo-ocular reflex (VOR) and visual fixation suppression of the VOR. This is like a window which allows you to look into the brain stem and cerebellum even if imaging is normal. Relevant anatomical structures are the midbrain, pons, medulla, cerebellum and rarely the cortex. There is a simple clinical rule: vertical and torsional eye movements are generated in the midbrain, horizontal eye movements in the pons. For example, isolated dysfunction of vertical eye movements is due to a midbrain lesion affecting the rostral interstitial nucleus of the medial longitudinal fasciculus (riMLF), with impaired vertical saccades only or vertical gaze-evoked nystagmus due to dysfunction of the Interstitial nucleus of Cajal (INC). Lesions of the lateral medulla oblongata (Wallenberg syndrome) lead to typical findings: ocular tilt reaction, central fixation nystagmus and dysmetric saccades. The cerebellum is relevant for almost all types of eye movements; typical pathological findings are saccadic smooth pursuit, gaze-evoked nystagmus or dysmetric saccades. The time course of the development of symptoms and signs is important for the diagnosis of underlying diseases: acute: most likely stroke; subacute: inflammatory diseases, metabolic diseases like thiamine deficiencies; chronic progressive: inherited diseases like Niemann-Pick type C with typically initially vertical and then horizontal saccade palsy or degenerative diseases like progressive supranuclear palsy. Treatment depends on the underlying disease. In this article, we deal with central ocular motor disorders. In a second article, we focus on clinically relevant types of nystagmus such as downbeat, upbeat, fixation pendular, gaze-evoked, infantile or periodic alternating nystagmus. Therefore, these types of nystagmus will not be described here in detail.

摘要

眼动障碍的诊断关键在于对不同类型的眼动进行系统的临床检查,包括眼位、自发性眼震、眼动范围、平滑追踪、扫视、固视功能、聚散、视动性眼震,以及前庭眼反射(VOR)功能和 VOR 视觉固视抑制的测试。这就像一扇窗户,即使影像学正常,也能让你观察到脑干和小脑。相关的解剖结构是中脑、脑桥、延髓、小脑,偶尔还有大脑皮层。有一个简单的临床规则:垂直和扭转眼动是由中脑产生的,水平眼动是由脑桥产生的。例如,孤立的垂直眼动功能障碍是由于中脑病变影响内侧纵束的间质核(riMLF)所致,仅表现为垂直扫视障碍或因 Cajal 间质核(INC)功能障碍导致垂直凝视诱发眼震。外侧延髓(Wallenberg 综合征)病变导致典型的发现:眼倾斜反应、中心固定性眼震和不等距扫视。小脑几乎与所有类型的眼动有关;典型的病理发现是扫视性平滑追踪、注视诱发眼震或不等距扫视。症状和体征的发展时间对潜在疾病的诊断很重要:急性:最有可能是中风;亚急性:炎症性疾病、硫胺素缺乏等代谢性疾病;慢性进行性:遗传性疾病,如尼曼-匹克 C 型,最初通常是垂直和水平扫视性瘫痪,或退行性疾病,如进行性核上性麻痹。治疗取决于潜在的疾病。在本文中,我们将讨论中枢性眼动障碍。在下一篇文章中,我们将重点介绍临床相关的眼震类型,如下跳性、上跳性、固定性摆动性、注视诱发性、婴儿型或周期性交替性眼震。因此,这里不会详细描述这些类型的眼震。

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