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脊髓空洞症及相关的Ⅰ型阿诺德-奇亚里畸形的计算机断层扫描

Computed tomography in syringomyelia and the associated Arnold-Chiari type I malformation.

作者信息

Forbes W S, Isherwood I

出版信息

Neuroradiology. 1978 Apr 27;15(2):73-8. doi: 10.1007/BF00334118.

Abstract

A total of 20 patients with an Arnold-Chiari Type I malformation, i.e. without skeletal abnormality and associated with a syringomyelic syndrome, were studied using the EMI Whole Body Scanner CT5000. Two groups were considered: (i) a retrospective series of 12 patients without intrathecal water soluble contrast media and (ii) a prospective series of eight patients after the introduction of intrathecal Metrizamide. In the first group tonsillar herniation could not be conclusively identified on CT and cord visualisation was possible in only two cases. In the second group, tonsillar herniation and cord expansion were consistently demonstrated. Cord cavitation has also been detected. In both groups it was possible to assess the size and position of the ventricular system. The results of this study indicate that evaluation of the upper cervical cord cerebellar tonsillar herniation, may be achieved, but only following opacification of the CSF. The precise extent of cerebellar tonsillar herniation may be difficult to evaluate. The reasons for these findings are discussed.

摘要

对20例患有I型阿诺德 - 基亚里畸形(即无骨骼异常且伴有脊髓空洞症综合征)的患者,使用EMI全身扫描仪CT5000进行了研究。分为两组:(i)回顾性系列中的12例患者未使用鞘内水溶性造影剂,(ii)前瞻性系列中的8例患者在引入鞘内甲泛葡胺后进行研究。在第一组中,CT上无法明确识别扁桃体疝,仅在两例中可见脊髓显影。在第二组中,始终显示出扁桃体疝和脊髓扩张。还检测到脊髓空洞形成。在两组中均能够评估脑室系统的大小和位置。本研究结果表明,只有在脑脊液显影后,才能对上颈段脊髓和小脑扁桃体疝进行评估。小脑扁桃体疝的确切范围可能难以评估。讨论了这些发现的原因。

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