Literature DB >> 17372858

A case of congenital high airway obstruction syndrome managed by ex utero intrapartum treatment: case report and review of the literature.

Fumi Shimabukuro1, Kaoru Sakumoto, Hitoshi Masamoto, Yoshihide Asato, Tomohide Yoshida, Akihiko Shinhama, Eiko Okubo, Aki Ishisoko, Yoichi Aoki.   

Abstract

Congenital high airway obstruction syndrome (CHAOS) has been reported to be fatal. Ten cases of CHAOS that underwent ex utero intrapartum treatment (EXIT) procedure to secure the fetal airway have been reported. A 36-year-old woman (gravida 3, para 2) was referred to our hospital at 22 weeks of gestation. Sonography revealed large echogenic lungs, flattened diaphragm, and marked hydrops. Magnetic resonance imaging confirmed the diagnosis of CHAOS. Polyhydramnios and fetal skin edema were improved and the fetal ascitic fluid was regressed gradually. At 36 weeks of gestation, an EXIT procedure was undertaken. Fetal laryngoscopy and bronchoscopy showed complete laryngeal obstruction, and a tracheostomy was performed immediately. The infant was discharged from hospital at 6 weeks of age. Thereafter, he developed well both physically and mentally. A laryngoplasty was performed at 20 months of age using silicon sheet as a patent airway. The child has a tracheostomy, is able to phonate but does not speak, and is awaiting decannulation. Use of the EXIT procedure in CHAOS cases offers the potential for salvage and excellent long-term outcome of these fetuses that otherwise would not survive. However, management of the airway, particularly with regard to long-term reconstruction in children with CHAOS, remains challenging.

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Year:  2007        PMID: 17372858     DOI: 10.1055/s-2007-972928

Source DB:  PubMed          Journal:  Am J Perinatol        ISSN: 0735-1631            Impact factor:   1.862


  7 in total

1.  Minimally invasive fetoscopic interventions: an overview in 2010.

Authors:  Thomas Kohl
Journal:  Surg Endosc       Date:  2010-03-17       Impact factor: 4.584

2.  Congenital high airway obstruction syndrome: MR/US findings, effect on management, and outcome.

Authors:  Andrew Mong; Ann M Johnson; Sandra S Kramer; Beverly G Coleman; Holly L Hedrick; Portia Kreiger; Alan Flake; Mark Johnson; R Douglas Wilson; N Scott Adzick; Diego Jaramillo
Journal:  Pediatr Radiol       Date:  2008-08-13

3.  Congenital laryngomucocoele: a rare cause for CHAOS.

Authors:  Manuel Sousa Cunha; Patrícia Janeiro; Rosário Fernandes; Helena Carreiro; Ricardo Laurini
Journal:  BMJ Case Rep       Date:  2009-02-27

4.  CHAOS: Prenatal imaging findings with post mortem contrast radiographic correlation.

Authors:  Kanika Gupta; Bhuvaneswari Venkatesan; Kiruba Shankar Manoharan; Vaithianathan Rajalakshmi; Maya Menon
Journal:  J Radiol Case Rep       Date:  2016-08-31

5.  Prenatal MRI findings of fetuses with congenital high airway obstruction sequence.

Authors:  Carolina V A Guimaraes; Leann E Linam; Beth M Kline-Fath; Lane F Donnelly; Maria A Calvo-Garcia; Eva I Rubio; Jeffrey C Livingston; Robert J Hopkin; Elizabeth Peach; Foong-Yen Lim; Timothy M Crombleholme
Journal:  Korean J Radiol       Date:  2009-03-03       Impact factor: 3.500

6.  MR imaging appearance of laryngeal atresia (congenital high airway obstruction syndrome): unique course in a fetus.

Authors:  Shigeko Kuwashima; Kazuhiro Kitajima; Yasushi Kaji; Hiroshi Watanabe; Yoshiyuki Watabe; Hiroshi Suzumura
Journal:  Pediatr Radiol       Date:  2007-12-11

7.  Postmortem magnetic resonance appearances of congenital high airway obstruction syndrome.

Authors:  Owen J Arthurs; Lyn S Chitty; Lydia Judge-Kronis; Neil J Sebire
Journal:  Pediatr Radiol       Date:  2014-09-05
  7 in total

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