Endoscopic Management of Esophageal Stenosis in Children with Congenital Esophageal Atresia

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منابع مشابه

Congenital Esophageal Stenosis Associated with Esophageal Atresia and Gasless Abdomen

SUMMARY A radiologically gasless abdomen in a neonate with EA is usually regarded as being pathognomonic of an absence of distal T.E.F. It has been estimated that up to 1.5% of patient with a distal fistula may have a radiologically gasless abdomens as a manifestation of a very small fistula plugged with mucus. In this case a contrast study via the gastrostomy demonstrated a fistula between th...

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Congenital esophageal stenosis associated with esophageal atresia.

Congenital esophageal stenosis (CES) is a rare clinical condition but is frequently associated with esophageal atresia (EA). The aim of this study is to report the diagnosis, management, and outcome of CES associated with EA. Medical charts of CES-EA patients from Lille University Hospital, Sainte-Justine Hospital, and Montreal Children's Hospital were retrospectively reviewed. Seventeen patien...

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Management of congenital esophageal stenosis.

BACKGROUND/PURPOSE The authors report the incidence, diagnosis, and treatment methods of congenital esophageal stenosis (CES) at their institution. METHODS A retrospective analysis of 123 patients with tracheoesophageal anomalies in a pediatric hospital between 1980 and 1999 was performed. Charts were reviewed for patient demographics, presence of true CES, associated congenital anomalies, me...

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Malnutrition and Feeding Problems in Children with Esophageal Atresia

Introduction: Esophageal atresia (EA) with or without tracheoesophageal fistula (TEF) is defined as a congenital malformation characterized with the interruption or obstruction of esophagus. Affected neonates may present with cyanosis during breast feeding, sialorrhea, coughing and difficulty in respiration. The defect should be corrected by surgery; otherwise, the condition ca...

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ژورنال

عنوان ژورنال: Advanced Research in Gastroenterology & Hepatology

سال: 2020

ISSN: 2472-6400

DOI: 10.19080/argh.2020.16.555929