[Brain stem dysfunction in Arnold-Chiari II syndrome].

A M Holschneider, J A Bliesener, M Abel
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引用次数: 9

Abstract

Among 76 patients suffering from myelomeningocele treated during 1978 to 1987 there were 12 children with brain stem signs as a sequel to Arnold-Chiari II syndrome. In 2 of these patients only stridor was seen, in 4 stridor with attacks of apnoea, in 2 attacks of apnoea with dysphagia, and in 4 children stridor, attacks of apnoea and dysphagia. Hence, it will be necessary to modify the classification given by Charney et al (4) in respect of brain stem patterns of signs according to three grades, since the signs of stridor, apnoea and dysphagia can be combined with each other in different ways. The prognosis is infaust if all 3 signs and hence grade III of brain stem lesions are present. On the whole, 6 out of 12 patients with brain stem signs died. For this reason, a possible Arnold-Chiari malformation should always be considered if stridor is observed, and, if necessary, early decompression treatment by means of a shunt revision should be performed.

[Arnold-Chiari II综合征的脑干功能障碍]。
在1978年至1987年期间治疗的76例脊髓脊膜膨出患者中,有12例儿童出现脑干体征,作为Arnold-Chiari II综合征的后遗症。其中2例患者仅出现喘鸣,4例喘鸣伴呼吸暂停发作,2例呼吸暂停伴吞咽困难发作,4例儿童喘鸣伴呼吸暂停和吞咽困难发作。因此,有必要对Charney等(4)将脑干体征模式分为三个等级进行修改,因为喘鸣、呼吸暂停和吞咽困难的体征可以以不同的方式组合在一起。如果所有3种体征均存在,则预后不良,因此脑干病变为III级。总体而言,12例脑干症状患者中有6例死亡。因此,如果观察到喘鸣,应始终考虑可能的Arnold-Chiari畸形,如有必要,应通过分流翻修进行早期减压治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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