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[一名21三体综合征患儿的阻塞性睡眠呼吸暂停综合征]

[Obstructive sleep apnea syndrome in a child with trisomy 21].

作者信息

Bloch K, Witztum A, Wieser H G, Schmid S, Russi E

机构信息

Medizinische Klinik, Universitätsspital Zürich.

出版信息

Monatsschr Kinderheilkd. 1990 Dec;138(12):817-22.

PMID:2150874
Abstract

Pulmonary hypertension without any cardiovascular malformation was diagnosed by heart catheterization in a 4 year old girl with trisomy 21. A suspected obstructive sleep apnea syndrome was confirmed by polysomnography which revealed numerous obstructive apneas and hypopneas (apnea-index 23/h) with marked oxygen desaturation and a disturbed sleep pattern. Three months after adenotonsillectomy the mother reported her daughter having a quiet sleep without snoring. Polysomnography did not show any apnea nor any oxygen desaturation below 90%. A decrease of the pulmonary artery pressure was documented. Facial dysmorphias and muscle hypotonia predispose patients with trisomy 21 to obstructive sleep apnea, especially if hypertrophy of tonsills and adenoids coexist. Frequent arousals and hypoxia during sleep can result in failure to thrive and pulmonary hypertension. These consequences can be prevented by early diagnosis and treatment.

摘要

一名患有21三体综合征的4岁女孩经心导管检查确诊为无任何心血管畸形的肺动脉高压。多导睡眠图证实疑似阻塞性睡眠呼吸暂停综合征,结果显示有大量阻塞性呼吸暂停和呼吸不足(呼吸暂停指数为23次/小时),伴有明显的氧饱和度下降和睡眠模式紊乱。腺样体扁桃体切除术后三个月,母亲报告女儿睡眠安静,无打鼾。多导睡眠图未显示任何呼吸暂停,也未显示氧饱和度低于90%。记录到肺动脉压力下降。面部畸形和肌张力减退使21三体综合征患者易患阻塞性睡眠呼吸暂停,尤其是在扁桃体和腺样体肥大并存的情况下。睡眠期间频繁觉醒和缺氧可导致发育不良和肺动脉高压。这些后果可通过早期诊断和治疗来预防。

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