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[眼球运动障碍中核上结构的生理病理学]

[The physiopathology of supranuclear structures in oculomotor disorders].

作者信息

Striano S, Luciano R, Meo R, Bilo L, Orefice G, Grasso A

机构信息

Universita Degli Studi, Napoli.

出版信息

Acta Neurol (Napoli). 1990 Apr;12(2):151-71.

PMID:2193486
Abstract

Several structures, located at different levels in the Central Nervous System (CNS), collaborate to the control and realization of ocular movements (O.M.) Therefore, alterations of oculomotricity, of varying degree and of different kinds, may be found in a lot of diseases of the CNS. The study of O.M., expecially when carried out by means of specific techniques such as electro-oculography, may represent an useful tool in the diagnosis (both from a topographic and an etiological standpoint) and in the follow-up of patients, possibly also allowing a precise evaluation of therapy effectiveness. In this review the Authors briefly examine the role of the supranuclear structures mostly involved in the control and in the execution of oculomotricity and the characteristics of the different types of O.M. (rapid and slow, vergence movements). Successively, they analyze the semeiological features of supra-nuclear disturbances of O.M., describing alterations of saccadic movements (slowing, dysmetria) and of smooth pursuit, fixation instability (square waves, flutter, opsoclonus, nystagmus,...) and other alterations of O.M. (ocular bobbing, see-saw nystagmus, skew deviation,...). Successively, disturbances of O.M. are analyzed in relation to their topodiagnostic significance, describing oculomotor involvements due to focal lesions of different areas of CNS (frontal cortex, parieto-occipital cortex, basal ganglia, cerebellum, brainstem) and particular syndromes (Foville syndromes, locked-in syndrome, Parinaud syndrome, anterior internuclear ophthalmoplegia, "one and a half" syndrome, Balint syndrome,...). Finally, particular attention is drawn to the oculomotor disturbances observed in degenerative cerebellar and multisystemic diseases, and several abnormal "oculomotor patterns", which seem to be specifically related to particular diseases, are described. In particular, the oculomotor patterns of Steele-Richardson-Olszewsky disease (slowing and hypometria of horizontal saccades, loss of upward saccades with preservation of reflex movements) and of Friedreich ataxia (fixation instability mostly due to the occurrence of square waves, saccadic dysmetria, impairment of smooth pursuit) are stressed.

摘要

位于中枢神经系统(CNS)不同水平的多个结构协同作用以控制和实现眼球运动(O.M.)。因此,在许多中枢神经系统疾病中都可能发现程度不同、类型各异的眼球运动功能障碍。对眼球运动的研究,尤其是通过眼电图等特定技术进行的研究,可能是诊断(从定位和病因学角度)以及患者随访中的有用工具,还可能有助于精确评估治疗效果。在这篇综述中,作者简要探讨了主要参与眼球运动控制和执行的核上结构的作用以及不同类型眼球运动(快速和慢速、辐辏运动)的特点。随后,他们分析了眼球运动核上紊乱的症状学特征,描述了扫视运动(减慢、辨距障碍)和平滑跟踪的改变、注视不稳定(方波、扑动、眼阵挛、眼球震颤等)以及其他眼球运动改变(眼球摆动、跷跷板样眼球震颤、斜视等)。接着,分析了眼球运动紊乱的定位诊断意义,描述了中枢神经系统不同区域(额叶皮质、顶枕叶皮质、基底神经节、小脑、脑干)局灶性病变以及特定综合征(福维尔综合征、闭锁综合征、帕里诺德综合征、前核间性眼肌麻痹、“一个半”综合征、巴林特综合征等)导致的眼球运动受累情况。最后,特别关注了在退行性小脑疾病和多系统疾病中观察到的眼球运动障碍,并描述了几种似乎与特定疾病具体相关的异常“眼球运动模式”。特别是,强调了斯蒂尔 - 理查森 - 奥尔谢夫斯基病的眼球运动模式(水平扫视减慢和幅度减小、向上扫视丧失但保留反射运动)和弗里德赖希共济失调的眼球运动模式(主要因方波出现导致的注视不稳定、扫视辨距障碍、平滑跟踪受损)。

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