An unusual case of esophageal and laryngotracheal atresia

Turk J Pediatr. Jan-Mar 2002;44(1):80-2.

Abstract

Esophageal atresia with or without tracheoesophageal fistula is a relatively common congenital anomaly. However, esophageal atresia with associated laryngotracheal atresia, double tracheoesophageal fistula and cardiac malformations is an extremely rare condition. In this article we report a newborn infant with severe respiratory distress at birth who had both esophageal and laryngotracheal atresia with congenital cardiac malformations, in an attempt to bring attention to the clinical presentation, and emergent diagnostic and therapeutic approaches.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple*
  • Esophageal Atresia / complications*
  • Fatal Outcome
  • Heart Defects, Congenital / complications
  • Humans
  • Infant, Newborn
  • Larynx / abnormalities*
  • Male
  • Respiratory Insufficiency / etiology
  • Trachea / abnormalities*