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羊膜镜辅助经皮气管和肺远端减压术逆转了先天性喉闭锁胎儿的羊水过多和胎儿窘迫。

Fetoscopy-Assisted Percutaneous Decompression of the Distal Trachea and Lungs Reverses Hydrops Fetalis and Fetal Distress in a Fetus with Laryngeal Atresia.

机构信息

Children's Hospital of Minnesota, Midwest Fetal Care Center, Minneapolis, Minnesota, USA.

Mayo Clinic, Division of Surgery Research, Rochester, Minnesota, USA.

出版信息

Fetal Diagn Ther. 2019;46(1):75-80. doi: 10.1159/000500455. Epub 2019 Jun 25.

Abstract

We present a case of prenatal hydrops secondary to congenital high airway obstruction syndrome (CHAOS) that was treated with fetoscopy-assisted needle decompression. A 22-year-old G3P2 woman presented after a 21-week ultrasound demonstrated CHAOS. The fetus developed hydrops at 25 weeks, characterized by abdominal ascites, pericardial effusion, and scalp edema. Fetal MRI showed complete obstruction of the glottis and subglottic airway, suggestive of laryngeal atresia. At 27 weeks, due to the progression of the hydrops, operative fetoscopy was proposed and performed. Fetal laryngoscopy confirmed fusion of the vocal cords and laryngeal atresia. The atretic segment was a solid cartilaginous block, preventing intubation. Using the fetoscope to stabilize the fetal head and neck, we performed ultrasound-guided percutaneous needle drainage of the cervical trachea through the anterior fetal neck. We removed 17 mL of viscous fluid from the lower trachea, resulting in immediate lung decompression. Two weeks later, ultrasound confirmed hydrops resolution. The patient was delivered and tracheostomy performed at 30 weeks via an ex utero intrapartum treatment (EXIT) procedure after progression of preterm labor. At 27 days of life, the infant was stable on minimal ventilator support. To our knowledge, this is the first successful report of an ultrasound-guided percutaneous tracheal decompression through the anterior neck of a fetus with CHAOS secondary to laryngeal atresia.

摘要

我们报告了一例产前水肿继发于先天性高位气道梗阻综合征(CHAOS)的病例,该病例通过胎儿镜辅助下的针减压治疗。一位 22 岁的 G3P2 女性在 21 周超声检查显示 CHAOS 后就诊。胎儿在 25 周时出现水肿,表现为腹腔积液、心包积液和头皮水肿。胎儿 MRI 显示声门和喉下气道完全梗阻,提示喉闭锁。在 27 周时,由于水肿的进展,提出并进行了手术性胎儿镜检查。胎儿喉镜检查证实声带融合和喉闭锁。闭锁段为实性软骨块,阻碍插管。我们使用胎儿镜稳定胎儿的头颈部,通过胎儿颈部前侧进行超声引导下经皮穿刺颈气管引流。我们从下气管中抽出 17 毫升粘性液体,立即使肺部减压。两周后,超声确认水肿消退。由于早产临产进展,患者在 30 周时通过宫外产时治疗(EXIT)程序分娩并进行了气管造口术。在 27 天时,婴儿在最小呼吸机支持下稳定。据我们所知,这是首例成功报告经胎儿颈部前侧超声引导下经皮气管减压治疗继发于喉闭锁的 CHAOS 的病例。

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