CONGENITAL ESOPHAGEAL WEB

نویسندگان
چکیده

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 distal esophageal obstruction caused by intraluminal mucosal web.

Here, we report a case with intraluminal membrane (web) located in the lower esophagus causing complete obstruction. Esophagogram revealed complete obstruction near the esophagogastric junction. Surgical excision of the esophageal membrane was performed. To our knowledge, only a few cases with membranous esophageal atresia have been reported. It must be remembered in neonates who cannot tolerat...

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CONGENITAL BRONCHO-ESOPHAGEAL FISTULA: A CASE REPORT

Congenital broncho-esophageal fistula (BEF) is a rare anomaly usually detected in adulthood. In one of the latest reviews of this anomaly, no more than 150 cases were found in the world literature. We report our experience with a 49 year old male patient referring with a classic presentation of chronic cough and choking episodes upon liquid intake. Broncho-esophageal fistula was confirmed b...

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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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Congenital esophageal stenosis.

Congenital esophageal stenosis CES is an uncommon anomaly that rarely goes undiagnosed until adulthood. We report 2 cases of CES. The first was a one-month-old baby boy who was referred for work up of swallowing disorder and recurrent pneumonias. The diagnosis was confirmed by a continuous fluoroscopic esophagogram, and endoscopic exploration. Simple dilatation resolved his symptoms completely....

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ژورنال

عنوان ژورنال: The Journal of Thoracic and Cardiovascular Surgery

سال: 1961

ISSN: 0022-5223

DOI: 10.1016/s0022-5223(20)31638-x