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An Ivor Lewis Esophagectomy Designed to Minimize Anastomotic Complications and Optimize Conduit Function
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An Ivor Lewis Esophagectomy Designed to Minimize Anastomotic Complications and Optimize Conduit Function

Published on: April 17, 2020

Upper esophageal stenosis: two case reports

S T Grabowski1, D A Andrews

  • 1Department of Surgery, St. Elizabeth Health Center, Youngstown, OH 44501-1790, USA.

Journal of Pediatric Surgery
|October 1, 1996
PubMed

Insights

Congenital esophageal stenosis is rare in children. Surgical web resection offered a lasting solution, while balloon dilatation required repeat treatments for strictures.

Area of Science:

  • Pediatric surgery
  • Gastroenterology

Background:

  • Congenital esophageal stenosis is an uncommon condition in pediatric patients.
  • Key forms include congenital esophageal webs, strictures from tracheobronchial remnants, and idiopathic muscular hypertrophy.

Observation:

  • Two pediatric cases of upper esophageal stenosis were successfully managed.
  • One patient had a congenital esophageal web, the other a congenital stricture.

Findings:

  • Successful surgical resection of the esophageal web resulted in no long-term dysphagia.
  • Balloon dilatation for esophageal stricture necessitated multiple repeat procedures.

Implications:

  • Surgical intervention may offer a definitive solution for congenital esophageal webs.
  • Congenital esophageal strictures might require long-term management strategies, including repeated dilatations.

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