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Problems Associated with Congenital Esophageal Atresia and Their Treatment

  • Pan Decker
  • J. Jakschik
  • C. H. Siebert
  • A. Hirner
Conference paper

Abstract

Congenital esophageal atresia is seen in 1 out of 3000 living births today. The cause of this malformation is a disturbance of the separation of the esophagus, trachea, and lung during their embryonic development. The resulting abnormalities have many different forms but can classified into five major groups as described by Gross-Vogt [1] (Fig. 1). During pregnancy, a hydramnion can frequently be noted, and the postpartum clinical consequences can include choking or coughing. Already during the first hours, the regurgitated gastric juices can pass into the lungs and cause chemical pneumonia and atelectasis. Therefore, an early diagnosis and proper treatment are of vital importance.

Keywords

Esophageal Stenosis Esophageal Atresia Tracheoesophageal Fistula Primary Suture Early Enteral Nutrition 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Tokyo 1993

Authors and Affiliations

  • Pan Decker
  • J. Jakschik
  • C. H. Siebert
  • A. Hirner
    • 1
  1. 1.Department of SurgeryUniversity of BonnBonn 1Germany

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