Esophageal motor function in congenital esophageal stenosis
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Updated: Aug 29, 2026

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Published on: August 11, 2023
Hisayoshi Kawahara1, Takaharu Oue, Hiroomi Okuyama
1Department of Pediatric Surgery, Osaka Medical Center and Research Institute for Maternal and Child Health, Izumi, Osaka, Japan.
Insights
Pediatric congenital esophageal stenosis (CES) is linked to gastroesophageal reflux and abnormal esophageal motility. This study investigated esophageal function in children with CES, finding common motor and reflux issues.
Area of Science:
- Pediatric Gastroenterology
- Esophageal Motility Disorders
- Congenital Anomalies
Background:
- Congenital esophageal stenosis (CES) is a rare condition causing foregut symptoms in infants and children.
- Understanding esophageal motor function in CES is crucial for diagnosis and management.
Purpose of the Study:
- To investigate esophageal motor function in pediatric patients diagnosed with isolated congenital esophageal stenosis (CES).
Main Methods:
- Study included four boys with CES (3 weeks to 4 years old) presenting with dysphagia or stridor.
- Evaluations included esophagram, endoscopy, 24-hour esophageal pH monitoring, and manometry.
- CES etiologies identified were fibromuscular stenosis (FMS), tracheobronchial remnants (TBR), and membranous diaphragm (MD).
Main Results:
- Esophagram revealed contrast stasis proximal to distal esophageal narrowing in FMS/TBR cases.
- No endoscopic esophagitis was observed.
- Three patients showed pathologic esophageal acid exposure; manometry indicated synchronous contractions in FMS/TBR patients and peristaltic waves in the MD patient.
- Incomplete lower esophageal sphincter (LES) relaxation occurred in FMS/TBR patients, though basal LES pressure was adequate.
Conclusions:
- Gastroesophageal reflux is prevalent in pediatric patients with CES.
- Impaired esophageal motility, including abnormal contractions and LES relaxation, is a common finding in CES.
Background/Purpose:
Congenital esophageal stenosis (CES) is a rare condition that is associated with various foregut symptoms. The aim of the current study was to investigate esophageal motor function in pediatric patients with isolated CES.
Methods:
Four boys with CES (age, 3 weeks to 4 years old) were studied before treatment. The initial symptoms were dysphagia or stridor. The CES was caused by fibromuscular stenosis (FMS) in 2, tracheobronchial remnants (TBR) in 1, and membranous diaphragm (MD) in 1. An esophagram, endoscopy, 24-hour esophageal pH monitoring, and manometry were conducted.
Results:
The esophagram showed the stasis of contrast medium proximally to the distal esophageal narrowing in FMS/TBR patients. Endoscopic esophagitis was not found in any patients. Three patients were documented with pathologic esophageal acid exposure by 24-hour esophageal pH monitoring. Manometry showed that esophageal contractions predominantly were synchronous in FMS/TBR patients but were peristaltic in an MD patient. Basal lower esophageal sphincter (LES) pressure was at least 20 mm Hg in all. Swallow-induced LES relaxations were incomplete in FMS/TBR patients.
Conclusions:
The presence of gastroesophageal reflux and impaired esophageal motility are common in patients with CES.
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