Double Trouble: A Rare Case of Dual Esophageal Stenosis in a 4-month-old

Amar Shah1, Ria Sharma1, Anirudh Shah1

  • 1Neonatal and Pediatric Surgeon, Amardeep Multispecialty Children Hospital and Research Centre, Ahmedabad, Gujarat, India.

Insights

Congenital esophageal stenosis (CES) is rare, affecting newborns. This case highlights a unique instance of a 4-month-old infant with multi-segment CES successfully treated with surgery.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Medical Genetics

Background:

  • Esophageal stenosis is a rare condition causing esophageal narrowing, present from birth (congenital) or acquired later.
  • Congenital esophageal stenosis (CES) occurs in 1 in 25,000-50,000 live births, often requiring early surgical intervention.
  • Multi-segment involvement is an exceptionally rare variant of CES.

Observation:

  • A 4-month-old infant presented with symptoms indicative of esophageal obstruction.
  • Diagnostic evaluation revealed stenosis affecting two distinct segments of the esophagus.
  • This presentation represents a rare anatomical variant of congenital esophageal stenosis.

Findings:

  • Surgical intervention was successfully performed to address the multi-segment esophageal stenosis.
  • The infant experienced a positive post-operative outcome.
  • This case underscores the importance of thorough diagnostic evaluation for CES.

Implications:

  • This case expands the understanding of congenital esophageal stenosis variants.
  • Successful surgical management of multi-segment CES provides a potential treatment pathway.
  • Further research into the etiology and management of rare CES variants is warranted.

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