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Erschienen in: Pediatric Surgery International 11/2005

01.11.2005 | Case Report

Communicating bronchopulmonary foregut malformation: particular emphasis on concomitant congenital tracheobronchial stenosis

verfasst von: Jiro Tsugawa, Chikara Tsugawa, Shiiki Satoh, Eiji Nishijima, Toshihiro Muraji, Shigeru Takamizawa, Kimio Kanegawa, Yoshinobu Akasaka

Erschienen in: Pediatric Surgery International | Ausgabe 11/2005

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Abstract

A total of four patients with communicating bronchopulmonary foregut malformation were treated surgically at Kobe Children’s Hospital between 1993 and 2004. Of these, three patients displayed congenital tracheobronchial stenosis and developed life-threatening respiratory distress soon after birth. In each case, anomalous bronchi arose from the lower portion of the esophagus and connected to the lower part of the ipsilateral lung. This anomaly involved the right lung in two patients, and the left lung in one patient. Tracheobronchial stenosis extended from the inlet of the thorax to the carina in one patient, and to the contralateral main stem bronchus in two patients. Surgical treatment included division of the esophageal bronchus and anastomosis of bronchus to the trachea in one patient. In the other patient, the ipsilateral lung was resected and the stenotic tracheobronchus was stented. The remaining patient underwent pneumonectomy of the ipsilateral lung. Details of this fatal anomaly and a discussion of appropriate surgical management are described herein.
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Metadaten
Titel
Communicating bronchopulmonary foregut malformation: particular emphasis on concomitant congenital tracheobronchial stenosis
verfasst von
Jiro Tsugawa
Chikara Tsugawa
Shiiki Satoh
Eiji Nishijima
Toshihiro Muraji
Shigeru Takamizawa
Kimio Kanegawa
Yoshinobu Akasaka
Publikationsdatum
01.11.2005
Verlag
Springer-Verlag
Erschienen in
Pediatric Surgery International / Ausgabe 11/2005
Print ISSN: 0179-0358
Elektronische ISSN: 1437-9813
DOI
https://doi.org/10.1007/s00383-005-1520-8

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