The Successful Treatment of Congenital Esophageal Stenosis by Endoscopic Dilatation

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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 duodenal web: successful management with endoscopic dilatation.

BACKGROUND AND STUDY AIMS Congenital duodenal web (CDW) is an uncommon cause of duodenal obstruction and endoscopic balloon dilatation has been reported in just eight pediatric cases to date. Here we are reporting three cases of CDW managed successfully with balloon dilatation. CASES AND METHODS In 2014 we diagnosed three cases of CDW on the basis of typical radiological and endoscopic findin...

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Successful endoscopic treatment (clipping) of esophageal perforation during balloon dilatation in a patient with achalasia.

woman with a 20−year history of inter− mittent dysphagia and regurgitation worsening over the past 6 years. The pa− tient underwent balloon dilatation as the first treatment of her disease. A Rigiflex balloon dilator (Boston Scientific, Boston, MA, USA) with a diameter of 30 mm was positioned over a guide wire at the gas− troesophageal junction under endoscopic control. An endoscope was introdu...

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INTRAMURAL TRACHEOBRONCHIAL REMNANTS: A MISDIAGNOSED CAUSE OF CONGENITAL ESOPHAGEAL STENOSIS

In cases of congenital esophageal stenosis due to tracheobronchial remnants, symptoms of partial esophageal obstruction appear at the time of weaning or during early childhood. In the absence of esophagitis, esophagram combined with cinefluoroscopy demonstrates fixed stenosis of distal esophagus and appears to be diagnostic. Dilatation of rigid stenosis is invariably unrewarding and surgic...

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Uncommon congenital antral web misdiagnosed twice as a pyloric ulcer: successful treatment with endoscopic balloon dilatation.

Congenital antral webs are quite rare and easily overlooked or misdiagnosed. We report the case of a five-year-old boy who presented with symptoms of gastric outlet obstruction for four years; his condition was misdiagnosed twice as pyloric ulcer. Detailed gastroscopy revealed a congenital antral web. The stricture was successfully treated with endoscopic balloon dilatation without surgery.

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ژورنال

عنوان ژورنال: The Journal of Pediatric Research

سال: 2016

ISSN: 2147-9445

DOI: 10.4274/jpr.28190