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Rapid Communication| Volume 47, ISSUE 10, e59-e62, October 2012

Congenital bronchopulmonary foregut malformation initially diagnosed as esophageal atresia type C: challenging diagnosis and treatment

  • Doeke Boersma
    Correspondence
    Corresponding author. Department of Paediatric Surgery, Emma Children's Hospital AMC, 1105 AZ, Amsterdam, The Netherlands. Tel.: +31 (0) 20 5665693; fax: +31 (0) 20 5669287.
    Affiliations
    Paediatric Surgical Centre of Amsterdam, Emma Children's Hospital AMC and VU University Medical Centre, Amsterdam, The Netherlands
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  • Bart G. Koot
    Affiliations
    Department of Paediatric Gastroenterology and Nutrition, Emma Children's Hospital AMC, Amsterdam, The Netherlands
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  • Erik Jonas van der Griendt
    Affiliations
    Department of Paediatric Respiratory Medicine and Allergy, Emma Children's Hospital AMC, Amsterdam, The Netherlands
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  • Author Footnotes
    1 Currently: Department of Surgery, Jeroen Bosch Ziekenhuis, Den Bosch, The Netherlands.
    Rick R. van Rijn
    Footnotes
    1 Currently: Department of Surgery, Jeroen Bosch Ziekenhuis, Den Bosch, The Netherlands.
    Affiliations
    Department of Radiology, Emma Children's Hospital AMC, Amsterdam, The Netherlands
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  • Alida F. van der Steeg
    Affiliations
    Paediatric Surgical Centre of Amsterdam, Emma Children's Hospital AMC and VU University Medical Centre, Amsterdam, The Netherlands
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  • Author Footnotes
    1 Currently: Department of Surgery, Jeroen Bosch Ziekenhuis, Den Bosch, The Netherlands.

      Abstract

      Communicating bronchopulmonary foregut malformations are extremely rare congenital malformations, characterized by a communicating fistula between an isolated part of the respiratory system and the esophagus or the stomach. In this article, we present a case of esophageal atresia type C, later diagnosed as a rare form of a communicating bronchopulmonary foregut malformation, an esophageal atresia combined with right main bronchus originating from the lower esophagus. Therapeutic resection of the right lung was complicated by postpneumonectomy syndrome.

      Key words

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