Successful tracheobronchial reconstruction of communicating bronchopulmonary foregut malformation and long segment congenital tracheal stenosis: a case report

Abstract Communicating bronchopulmonary foregut malformation (CBPFM) and congenital tracheal stenosis (CTS) are difficult developmental disorders especially when they are presented simultaneously in a patient. The authors report a case of a newborn boy born at 37 weeks of gestation weighing 2356 g w...

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Veröffentlicht in:Journal of pediatric surgery 2012-09, Vol.47 (9), p.e41-e46
Hauptverfasser: Takamizawa, Shigeru, Yoshizawa, Katsumi, Machida, Mizuho, Iwade, Tamaki, Abe, Seiki, Ohata, Jun, Takahashi, Daijiro, Nishijima, Eiji
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Sprache:eng
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Zusammenfassung:Abstract Communicating bronchopulmonary foregut malformation (CBPFM) and congenital tracheal stenosis (CTS) are difficult developmental disorders especially when they are presented simultaneously in a patient. The authors report a case of a newborn boy born at 37 weeks of gestation weighing 2356 g with CBPFM (right esophageal lung) and long segment CTS. Staged surgical repair (by-force endotracheal intubation for securing the airway followed by bronchotracheal anastomosis for CBPFM, tracheostomy with handmade, length-adjustable tracheostomy tube, and slide tracheoplasty) was performed. He has been healthy without tracheostomy for 25 months after slide tracheoplasty. This is the first report of a successful tracheobronchial reconstruction for a patient with a long segment CTS and CBPFM preserving the affected lung function.
ISSN:0022-3468
1531-5037
DOI:10.1016/j.jpedsurg.2012.06.009