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Congenital high airway obstruction syndrome (CHAOS) combined with esophageal atresia, tracheoesophageal fistula and duodenal atresia

Authors :
Yutaka Kanamori
Toshiko Takezoe
Kazunori Tahara
Toshihiko Watanabe
Michinobu Ohno
Kotaro Tomonaga
Katsuhiro Ogawa
Tomoro Hishiki
Akihiro Fujino
Yuri Ozawa
Shoichiro Amari
Hideshi Fujinaga
Yushi Ito
Osamu Miyazaki
Noriko Morimoto
Rika Sugibayashi
Katsusuke Ozawa
Seiji Wada
Haruhiko Sago
Source :
Journal of Pediatric Surgery Case Reports, Vol 26, Iss C, Pp 22-25 (2017)
Publication Year :
2017
Publisher :
Elsevier, 2017.

Abstract

Congenital high airway obstruction syndrome (CHAOS) is a rare congenital anomaly and the most common etiology is laryngeal atresia. Recently, an increasing number of cases have survived due to prenatal diagnosis and pre- and peri-natal care including ex-utero intrapartum treatment (EXIT). More than 100 cases of CHAOS have been reported, and about half of them were complicated with associated anomalies. Here we report a very rare case of prenatally diagnosed CHAOS (laryngeal atresia) complicated with esophageal atresia, tracheoesophageal fistula (TEF) and duodenal atresia, and the patient was saved by EXIT. This combination of anomalies resulted in a very confusing prenatal diagnosis with unique imaging feature of the fetus.

Details

Language :
English
ISSN :
22135766
Volume :
26
Issue :
C
Database :
Directory of Open Access Journals
Journal :
Journal of Pediatric Surgery Case Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.16640cebfc24f558c8af56edeca476b
Document Type :
article
Full Text :
https://doi.org/10.1016/j.epsc.2017.08.021