Journal of Pediatric Surgery Case Reports (Nov 2017)

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

  • 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

DOI
https://doi.org/10.1016/j.epsc.2017.08.021
Journal volume & issue
Vol. 26, no. C
pp. 22 – 25

Abstract

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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.

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