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Transient mega-esophagus in a neonate with congenital diaphragmatic hernia

I R Makhoul1, G Shoshany, T Smolkin

  • 1Department of Neonatology, Rambam Medical Center and Rappaport Faculty of Medicine, Technion, Bat-Galim 31096, Haifa, Israel. makhoul@rambam.health.gov.il

European Radiology
|May 25, 2001
PubMed

Insights

Esophageal dilatation in neonates is rare but can occur with congenital diaphragmatic hernia. This condition often resolves with conservative management, as seen in this case study.

Area of Science:

  • Neonatal Medicine
  • Pediatric Surgery
  • Gastroenterology

Background:

  • Esophageal dilatation (ED) is a rare condition in neonates.
  • Congenital diaphragmatic hernia (CDH) is a serious birth defect affecting lung development.

Observation:

  • A term neonate post-CDH repair presented with ED detected on chest radiograph.
  • Swallow studies revealed ED, a sub-diaphragmatic stomach, and later, gastroesophageal reflux with a small hiatus hernia.

Findings:

  • The fetal herniated stomach likely caused gastroesophageal junction obstruction, leading to ED and concealed reflux.
  • The infant showed adequate thriving on enteral feeding despite the initial findings.

Implications:

  • Highlights the association between ED and CDH, emphasizing the need for clinical awareness.
  • Suggests a benign course for ED associated with CDH when managed conservatively.

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