TY - JOUR
T1 - Congenital bronchopulmonary foregut malformation initially diagnosed as esophageal atresia type C: challenging diagnosis and treatment
AU - Boersma, Doeke
AU - Koot, Bart G.
AU - van der Griendt, Erik Jonas
AU - van Rijn, Rick R.
AU - van der Steeg, Alida F.
PY - 2012
Y1 - 2012
N2 - 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. (C) 2012 Elsevier Inc. All rights reserved
AB - 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. (C) 2012 Elsevier Inc. All rights reserved
U2 - https://doi.org/10.1016/j.jpedsurg.2012.07.060
DO - https://doi.org/10.1016/j.jpedsurg.2012.07.060
M3 - Article
C2 - 23084235
SN - 0022-3468
VL - 47
SP - E59-E62
JO - Journal of pediatric surgery
JF - Journal of pediatric surgery
IS - 10
ER -