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Conditional Reprogramming of Pediatric Human Esophageal Epithelial Cells for Use in Tissue Engineering and Disease Investigation
Published on: March 22, 2017
Congenital esophageal webs
P C Patel1, J A Yates, W S Gibson
1Department of Otolaryngology-Head and Neck Surgery, Geisinger Medical Center, Danville, PA 17822-1333, USA.
Insights
Congenital esophageal webs are rare causes of childhood feeding difficulties. This study reviews two pediatric cases, detailing the pathophysiology, diagnosis, and management of these upper esophageal lesions.
Area of Science:
- Pediatric Gastroenterology
- Congenital Malformations
Background:
- Congenital esophageal webs are uncommon developmental anomalies.
- Typically located in the upper esophagus, they manifest in early childhood.
Observation:
- Symptoms include dysphagia and significant feeding challenges.
- Radiography often shows a thin, anterior, or circumferential indentation of the esophageal lumen.
Findings:
- This report details two pediatric cases of congenital esophageal webs.
- The review covers the underlying pathophysiology, diagnostic approaches, and treatment strategies.
Implications:
- Understanding these rare anomalies is crucial for timely diagnosis and intervention.
- Effective management can significantly improve outcomes for affected children.
Abstract:
Congenital esophageal webs are rare entities. These lesions generally occur in the upper one third of the esophagus and present symptomatically in early childhood. Dysphagia and 'feeding' difficulties are characteristic presenting symptoms. Radiographic studies generally reveal a normal appearing esophageal lumen with the exception of a single thin indentation of the esophageal lumen that is located either anteriorly or circumferential in nature. We describe two children with congenital esophageal webs and review the pathophysiology, diagnosis and management of these unusual lesions.
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