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眼球运动所揭示的Chiari II型畸形的小脑发育不全

The cerebellar dysplasia of Chiari II malformation as revealed by eye movements.

作者信息

Salman Michael S, Dennis Maureen, Sharpe James A

机构信息

Children's Hospital, University of Manitoba, Winnipeg, Manitoba, Canada.

出版信息

Can J Neurol Sci. 2009 Nov;36(6):713-24. doi: 10.1017/s0317167100008325.

Abstract

INTRODUCTION

Chiari type II malformation (CII) is a developmental deformity of the hindbrain. We have previously reported that many patients with CII have impaired smooth pursuit, while few make inaccurate saccades or have an abnormal vestibuloocular reflex. In contrast, saccadic adaptation and visual fixation are normal. In this report, we correlate results from several eye movement studies with neuroimaging in CII. We present a model for structural changes within the cerebellum in CII.

METHODS

Saccades, smooth pursuit, the vestibulo-ocular reflex, and visual fixation were recorded in 21 patients with CII, aged 8-19 years and 39 age-matched controls, using an infrared eye tracker. Qualitative and quantitative MRI data were correlated with eye movements in 19 CII patients and 28 controls.

RESULTS

Nine patients with CII had abnormal eye movements. Smooth pursuit gain was subnormal in eight, saccadic accuracy abnormal in four, and vestibulo-ocular reflex gain abnormal in three. None had fixation instability. Patients with CII had a significantly smaller cerebellar volume than controls, and those with normal eye motion had an expanded midsagittal vermis compared to controls. However, patients with abnormal eye movements had a smaller (non-expanded) midsagittal vermis area, posterior fossa area and medial cerebellar volumes than CII patients with normal eye movements.

CONCLUSIONS

The deformity of CII affects the structure and function of the cerebellum selectively and differently in those with abnormal eye movements. We propose that the vermis can expand when compressed within a small posterior fossa in some CII patients, thus sparing its ocular motor functions.

摘要

引言

Chiari II型畸形(CII)是一种后脑发育畸形。我们之前报道过,许多CII患者的平稳跟踪受损,而很少有人扫视不准确或前庭眼反射异常。相比之下,扫视适应和视觉注视是正常的。在本报告中,我们将多项眼动研究结果与CII患者的神经影像学结果进行关联。我们提出了一个CII患者小脑结构变化的模型。

方法

使用红外眼动追踪仪记录了21例年龄在8至19岁的CII患者以及39例年龄匹配的对照者的扫视、平稳跟踪、前庭眼反射和视觉注视情况。对19例CII患者和28例对照者的定性和定量MRI数据与眼动情况进行了关联分析。

结果

9例CII患者存在眼动异常。8例患者的平稳跟踪增益低于正常水平,4例患者的扫视准确性异常,3例患者的前庭眼反射增益异常。无一例存在注视不稳定情况。CII患者的小脑体积明显小于对照者,眼动正常的患者与对照者相比,其矢状位小脑蚓部增大。然而,眼动异常的患者与眼动正常的CII患者相比,其矢状位小脑蚓部面积、后颅窝面积和小脑内侧体积更小。

结论

CII畸形对小脑结构和功能的影响具有选择性,且在眼动异常的患者中表现不同。我们提出,在一些CII患者中,当小脑蚓部在狭小的后颅窝内受到挤压时,它可以扩张,从而保留其眼球运动功能。

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