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Congenital cystic adenomatoid malformation of the lung associated with esophageal atresia and tracheoesophageal fistula

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Abstract

Bronchopulmonary malformations associated with esophageal atresia (EA) and tracheoesophageal fistula (TEF) are extremely rare. The authors describe a case of type II congenital cystic adenomatoid malformation (CCAM) of the right lower lobe associated with EA and TEF (Vogt-Gross type C) in a full-term female infant. The CCAM presented as an incidental radiologic finding, and a contralateral tension pneumothorax developed shortly after surgical repair of the EA. Early recognition of this rare association is essential for correct operative management.

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Authors and Affiliations

  1. Institute of Preventive Pediatrics and Neonatology, University of Siena, Italy, , , , , , IT

    C. De Felice, F. Bagnoli & R. Bracci

  2. Department of Pediatric Surgery, University of Siena, Italy, , , , , , IT

    G. Di Maggio, M. Messina & G. Tota

  3. Institute of Pathology, University of Siena, Italy, , , , , , IT

    P. Toti

Authors
  1. C. De Felice
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  2. G. Di Maggio
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  3. M. Messina
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  4. P. Toti
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  5. F. Bagnoli
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  6. R. Bracci
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  7. G. Tota
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Accepted: 26 May 1998

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De Felice, C., Di Maggio, G., Messina, M. et al. Congenital cystic adenomatoid malformation of the lung associated with esophageal atresia and tracheoesophageal fistula. Pediatr Surg Int 15, 260–263 (1999). https://doi.org/10.1007/s003830050571

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  • DOI: https://doi.org/10.1007/s003830050571

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