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颅底发育不良与 Chiari Ⅰ型畸形和脊髓空洞症相关。

Clival dysgenesis associated with Chiari Type 1 malformation and syringomyelia.

机构信息

Department of Neurosurgery, King Edward Memorial Hospital and Seth G. S. Medical College, Acharya Donde Marg, Parel, Mumbai 400012, India.

出版信息

J Clin Neurosci. 2010 Mar;17(3):400-1. doi: 10.1016/j.jocn.2009.05.031. Epub 2010 Jan 13.

DOI:10.1016/j.jocn.2009.05.031
PMID:20074957
Abstract

We report an 11-year-old boy with dysgenesis of the clivus. The boy presented complaining of progressive difficulty in walking. The clival anomaly was associated with severe basilar invagination, Chiari Type 1 malformation and syringomyelia. Our literature search did not reveal any previous reports of this combination of conditions. The patient obtained relief from his symptoms following a foramen magnum decompression.

摘要

我们报告了一例 11 岁的颅底发育不良男孩。该男孩主诉进行性行走困难。颅底异常与严重的颅底凹陷症、Chiari Ⅰ型畸形和脊髓空洞症有关。我们的文献检索未发现以前有任何关于这种组合病症的报告。患者在进行了枕骨大孔减压手术后，症状得到缓解。

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