Objectives: After surgical repair, up to 70% of esophageal atresia (EA) patients suffer from
gastroesophageal reflux disease (GERD). The ESPGHAN/NASPGHAN guidelines on …

Purpose To estimate the incidence, mortality and cancer risk of the congenital malformation
esophageal atresia (EA) in a population-based investigation. Methods A population-based …

Objectives Endoscopic follow-up after esophageal atresia (EA) tracheoesophageal fistula
(TEF) repair is recommended to detect esophageal histopathological complications. We …

Introduction Because many aspects of the management of esophageal atresia (EA) are still
controversial, we evaluated the practice patterns of this condition across Europe. Methods A …

Purpose A prospective national register was established in 2008 to record all new cases of
live-birth newborns with esophageal atresia (EA). This epidemiological survey was …

BACKGROUND: Gastroesophageal reflux is a frequent problem after esophageal atresia
(EA) repair. Our aim was to determine the prevalence of esophagitis and Barrett esophagus …

Esophageal atresia (EA) is a rare congenital malformation consisting of a lack of continuity
between the upper and lower esophageal pouches, frequently associated with …

Objective: Postoperative morbidity after correction of esophageal atresia is partly determined
by gastroesophageal reflux disease, which has been proven to affect from one-half to two …

Background Esophageal atresia (EA) is a life-threatening congenital condition, affecting one
in 2600 newborns. Morbidity remains high, with many patients experiencing complications …

We report a case of esophageal adenocarcinoma 20 years after esophageal atresia repair.
From one case report it is premature to recommend cancer surveillance for all esophageal …