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Incomplete duplication of the esophagus: a case report

Piyawan Chiengkriwate1, Sakda Patrapinyokul, Chareonkiat Rergkliang

  • 1Pediatric Surgery Unit, Department of Surgery, Faculty of Medicine, Prince of Songkla University, Hat-Yai, Songkla 90110, Thailand. chiengkriwate_piyawan@hotmail.com

Journal of the Medical Association of Thailand = Chotmaihet Thangphaet
|January 13, 2006
PubMed

Insights

Incomplete esophageal duplication was diagnosed in a 20-month-old girl with esophageal perforation. Surgical resection of the duplication effectively treated the condition.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Congenital Abnormalities

Background:

  • Esophageal duplication cysts are rare congenital anomalies.
  • They can present with various symptoms, including esophageal perforation.

Observation:

  • A 20-month-old girl presented with symptoms of esophageal perforation.
  • Imaging revealed pneumomediastinum and subcutaneous emphysema.
  • Contrast esophagography showed leakage from the cervical esophagus.

Findings:

  • The patient was diagnosed with incomplete duplication of the esophagus.
  • Endoscopic examination provided further diagnostic details.
  • Complete surgical resection of the esophageal duplication was performed.

Implications:

  • This case highlights the importance of considering esophageal duplication in pediatric patients with esophageal perforation.
  • Successful surgical management can lead to a favorable outcome.
  • Early diagnosis and intervention are crucial for managing this rare condition.

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