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Updated: May 20, 2026

Robotic Myotomy and Partial Fundoplication for Achalasia
Published on: August 11, 2023
Achalasia cardia in a premature infant
Naveen Shettihalli1, Vikranth Venugopalan, Nicholas Kevin Ives
1Department of Neonatology, John Radcliffe Hospital, Oxford, UK. drnaveenshettihalli@rediffmail.com
Insights
Achalasia cardia, a rare esophageal motility disorder, was diagnosed in a preterm infant, an unprecedented case. Successful treatment involved Heller
Area of Science:
- Pediatric Gastroenterology
- Esophageal Motility Disorders
Background:
- Achalasia cardia is a neuromuscular esophageal disorder characterized by abnormal motility and impaired relaxation of the lower esophageal sphincter.
- While recognized in infants and children, achalasia in preterm neonates remains undescribed.
Observation:
- This report details the first documented case of achalasia cardia in a premature infant.
- The infant presented with an atypical clinical manifestation of the condition.
Findings:
- The premature infant diagnosed with achalasia cardia showed successful management.
- Treatment involved a surgical approach: Heller's esophagomyotomy combined with fundoplication.
Implications:
- This case expands the understanding of achalasia cardia's occurrence in neonatology.
- It highlights the feasibility of surgical intervention for this rare condition in preterm infants.
Abstract:
Achalasia cardia is defined as a neuromuscular disorder of the oesophagus with abnormal motility and failure of relaxation of the distal oesophagus. It is an uncommon but well-recognised entity in infants and children. However, achalasia in a preterm baby has not been previously described. We report the condition in a premature infant with unusual presentation, treated successfully with Heller's oesophagomyotomy and fundoplication.
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