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Chiari I 畸形的历史、解剖形态及发病机制。

History, anatomic forms, and pathogenesis of Chiari I malformations.

作者信息

Schijman Edgardo

机构信息

Section of Neurosurgery, Hospital C. Durand, Buenos Aires, Argentina.

出版信息

Childs Nerv Syst. 2004 May;20(5):323-8. doi: 10.1007/s00381-003-0878-y. Epub 2004 Feb 5.

Abstract

INTRODUCTION

Chiari I malformations constitute a group of entities of congenital or acquired etiology that have in common descent of the cerebellar tonsils into the cervical spinal canal. In recent years, since the advent of magnetic resonance imaging, an increasing number of asymptomatic, doubtfully symptomatic, and minimally symptomatic patients with Chiari I malformations have been diagnosed. This has resulted in controversy about the multiple therapeutic strategies indicated for these problems.

OBJECT

With the intention of updating the knowledge that we currently have on the Chiari I malformation and the related syringomyelia we review the literature and discuss the historical background, pathogenesis, anatomic forms, clinical presentation, and diagnostic procedures of these abnormalities.

摘要

引言

Chiari I畸形是一组先天性或后天性病因的疾病,其共同特征是小脑扁桃体下疝至颈椎管内。近年来,自磁共振成像问世以来,越来越多无症状、可疑症状及症状轻微的Chiari I畸形患者被诊断出来。这引发了针对这些问题的多种治疗策略的争议。

目的

为更新我们目前对Chiari I畸形及相关脊髓空洞症的认识,我们回顾了文献,并讨论了这些异常情况的历史背景、发病机制、解剖形式、临床表现及诊断方法。

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