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

被引：9

作者：

De Felice, C ^{[1
]}

Di Maggio, G ^{[1
]}

Messina, M ^{[1
]}

Toti, P ^{[1
]}

Bagnoli, F ^{[1
]}

Bracci, R ^{[1
]}

Tota, G ^{[1
]}

机构：

[1] Univ Siena, Inst Prevent Pediat & Neonatol, I-53100 Siena, Italy

来源：

PEDIATRIC SURGERY INTERNATIONAL | 1999年 / 15卷 / 3-4期

关键词：

esophageal atresia; tracheoesophageal fistula; congenital cystic adenomatoid malformation pneumothorax; newborn;

D O I：

10.1007/s003830050571

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

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.

引用

页码：260 / 263

页数：4

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