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[1例伴有睡眠呼吸暂停的Ⅰ型阿诺德-奇亚里畸形患者猝死]

[A sudden-death in a case of Arnold-Chiari malformation (type I) with sleep apnea].

作者信息

Iwabuchi K, Miyauchi T, Kyuuma Y, Hosaka H, Kunimi Y, Yagishita S

出版信息

No To Shinkei. 1985 Jun;37(6):575-81.

PMID:4041288
Abstract

UNLABELLED

We presented a sudden-death case of Arnold-Chiari malformation (type 1) accompanied with spina bifida and closed meningomyelocele. Polysomnography revealed the increase of both central and mixed type apneas to compare with the findings of typical Pickwikian syndrome.

THE CASE

30-year-old female without obese or obstruction of upper air way. Spina bifida and closed meningomyelocele at sacral portion were found at her birth. She had no treatment and had not been able to walk because of paralysis at low extremities. Since she was 25-year-old, she had had insomnia which accompanied by choked feelings, palpitations, clumsiness of hands and anxiety. Snoring was light, and she had neither respiratory disturbances nor hypersomnia during awake. She was admitted to our hospital for treatment of decubitus. 2nd June, 1977, she was found acrocyanosis during sleep and immediately she was resurrected. Physical examinations revealed there was no accounting for sudden respiratory arrest: the cardio-pulmonary system was normal during awake and laboratory findings also failed to disclose the episode. But she had slight dysfunctions of lower cranial nerves: fine nystagmus according to the head-position, decreased gag reflex, and paresis in the recurrence nerve of N.XII and etc. Angiography showed communicating hydrocephalus. Though ventriculoperitoneal shunt operation was performed at 8th June, sleep apnea could not be improved. Therefore we examined in order to clarify her sleep apnea. She was not obese, we could not find any obstructions of upper air way. Nocturnal polygraphy was performed at 8th July. The results were summarized as follows: (1) Total sleep time was 293 minutes and numbers of sleep apnea were 134 times.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

未标注

我们报告了一例伴有脊柱裂和隐性脊髓脊膜膨出的阿诺德 - 奇亚里畸形(1型)猝死病例。多导睡眠图显示,与典型的匹克威克综合征相比,中枢性和混合型呼吸暂停均增加。

病例

一名30岁女性,无肥胖或上气道阻塞。出生时发现骶部脊柱裂和隐性脊髓脊膜膨出。她未接受治疗,因下肢瘫痪无法行走。自25岁起,她出现失眠,伴有窒息感、心悸、手部笨拙和焦虑。打鼾较轻,清醒时既无呼吸障碍也无嗜睡。她因褥疮入院治疗。1977年6月2日,睡眠中发现她肢端青紫,随后立即复苏。体格检查显示无法解释突然的呼吸骤停:清醒时心肺系统正常,实验室检查结果也未能揭示该发作情况。但她有轻微的下颅神经功能障碍:根据头部位置出现细微眼球震颤、咽反射减弱以及舌下神经回返神经麻痹等。血管造影显示交通性脑积水。尽管6月8日进行了脑室腹腔分流手术,但睡眠呼吸暂停仍未改善。因此,为明确她的睡眠呼吸暂停情况进行了检查。她不肥胖,未发现上气道有任何阻塞。7月8日进行了夜间多导睡眠监测。结果总结如下:(1)总睡眠时间为293分钟,睡眠呼吸暂停次数为134次。(摘要截断于250字)

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