Esophageal Atresia with Double Tracheoesophageal Fistula: A Case Report

Author(s):  
So Hyun Nam ◽  
Dae Yeon Kim ◽  
Seong Chul Kim ◽  
In Koo Kim
2016 ◽  
Vol 5 (3) ◽  
pp. 32 ◽  
Author(s):  
Rossella Angotti ◽  
Francesco Molinaro ◽  
Anna Lavinia Bulotta ◽  
Francesco Ferrara ◽  
Marina Sica ◽  
...  

More than 50% of infants with esophageal atresia have associated anomalies. We present a case report of a 46XX neonate with long-gap esophageal atresia and tracheoesophageal fistula (EA/TEF), anorectal malformation, bowel duplication and vaginal agenesis. This is an unusual association of abnormalities which had not yet described in literature.


2015 ◽  
Vol 05 (02) ◽  
pp. 147-150
Author(s):  
Bijay Upadhyay ◽  
Xuedong Wu ◽  
Jun Li ◽  
Ning Wang ◽  
Shanshan Zhang ◽  
...  

2005 ◽  
Vol 15 (5) ◽  
pp. 354-357 ◽  
Author(s):  
S. Katsura ◽  
T. Shono ◽  
T. Yamanouchi ◽  
T. Taguchi ◽  
S. Suita

2006 ◽  
Vol 59 (1-2) ◽  
pp. 73-78 ◽  
Author(s):  
Svetlana Bukarica ◽  
Smiljana Marinkovic ◽  
Vladimir Borisev ◽  
Jelena Antic

We present a case report of a neonate with esophageal atresia and tracheoesophageal fistula. In the 31st week of gestation, maternal polyhydramnions was observed by prenatal ultrasonography. Postnatal insertion of an orogastric tube into the stomach was unsuccessful. On auscultation, the apex of the heart was heard at the right side of the thorax, while the liver was palpable I cm below the left rib cage. Esophageal atresia with tracheoesphageal fistula and situs inversus of the thoracic and abdominal organs was diagnosed. During the first day of life, left transpleural thoracotomy was performed. The fistula was closed and esophageal anastomosis performed. One year after the operation the child had no difficulties when eating solid and liquid foods. More than 50% of infants with esophageal atresia have associated anomalies and the esophagogram showed good passage of contrast with anastomotic stricture. This was the first report of esophageal atresia with tracheoesophageal fistula repair in a patient with situs inversus treated in our Clinic. .


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