[先天性高气道阻塞综合征(CHAOS)胎儿的诊断和处理]。

Q3 Medicine
Revue medicale de Liege Pub Date : 2023-02-01
Camille Jaminet, Francoise Leonard, Roland Devlieger, Frederic Chantraine
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引用次数: 0

摘要

先天性高气道阻塞综合征是一种罕见的畸形,如果不进行围产期干预,其预后很差,可能导致胎儿或围产期死亡。然而,超声和磁共振使准确的产前诊断和最佳选择的介入胎儿医学技术(经气管穿刺,胎儿镜检查)。这些方法减少了与病理过程相关的胎儿副作用,避免了母体宫内治疗及其有害影响。如果它成为不可缺少的宫内治疗,可以通过保护胎儿气道来优化新生儿的管理,同时通过维持母婴循环将缺氧损伤的风险降至最低。我们报告一对夫妇在闭经21周时出现疑似CHAOS病例,诊断和处理直到孩子出生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Diagnosis and management of a foetus with congenital high airway obstruction syndrome (CHAOS)].

Congenital high airway obstruction syndrome is a rare malformation whose prognosis is very poor resulting in foetal or perinatal death if no perinatal intervention is performed. However, ultrasound and magnetic resonance enable an accurate prenatal diagnosis and optimal choice of interventional foetal medicine techniques (transtracheal puncture, fetoscopy). These approaches reduce foetal side effects related to the pathological process, and avoid the mother ex utero intrapartal treatment and its deleterious effects. If it becomes indispensable ex utero intrapartal treatment allows optimal management of the new born by securing the foetal airways while minimizing risk for hypoxic damage through the maintenance of maternal-foetal circulation. We present the story of a couple with a suspected case of CHAOS at 21 weeks of amenorrhea, the diagnostic and the management until the birth of the child.

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来源期刊
Revue medicale de Liege
Revue medicale de Liege Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
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0
期刊介绍: The Medical Review of Liege is a tool for continuous medical training being addressed to students, general practitioners, and specialists
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