Arnold-Chiari畸形——近距离观察。

P R Guin
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引用次数: 10

摘要

Arnold-Chiari畸形(ACM)是一种颈髓交界处的畸形,其特征是小脑扁桃体、脑干和第四脑室向颈上管移位。这种异常的临床表现在很大程度上取决于发病年龄、相关病理和有无脊髓灰质炎。关于Arnold-Chiari畸形的发病机制、体征、症状、诊断和成功治疗,文献中存在相当大的争议。本文将探讨这些问题,并讨论该综合征患者的护理管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Arnold-Chiari malformation--a closer look.

Arnold-Chiari malformation (ACM) is a malformation of the cervico-medullary junction characterized by displacement of the cerebellar tonsils, the brainstem and the fourth ventricle into the upper cervical canal. The clinical presentation of this anomaly is largely dependent upon age at onset, associated pathology, and the presence of hydromyelia. Considerable controversy exists within the literature concerning pathogenesis, signs and symptoms, diagnosis, and successful treatment of Arnold-Chiari malformation. This article will examine these issues and discuss the nursing management of patients with this syndrome.

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