Esophageal Columnar Metaplasia in Childhood: A Population-Based Case Series Analysis.

Dig Dis Sci

Department of Gastroenterology, Belfast Health and Social Care Trust, Belfast, Northern Ireland, UK.

Published: July 2021

AI Article Synopsis

  • Pediatric Barrett's esophagus (BE) is rare, with only 42 cases identified in Northern Ireland from 1993 to 2010, equating to an incidence of less than 2 per 100,000 children.
  • Most of the pediatric BE patients were male (85.7%), indicating a significant gender difference compared to adult cases.
  • None of the pediatric patients progressed to high-grade dysplasia or esophageal adenocarcinoma, suggesting that routine surveillance for these conditions might not be necessary until they reach adulthood.

Article Abstract

Background: Adults with Barrett's esophagus (BE) are often entered into surveillance for esophageal adenocarcinoma (EAC), although cancer risk is relatively low. BE can be detected in children (< 16 years). Little is known about the epidemiology of pediatric BE, and it is unclear what the optimal surveillance regimes are in children.

Aim: To evaluate the demographic and clinical characteristics, and future neoplastic progression risk in all pediatric BE patients diagnosed in Northern Ireland between 1993 and 2010.

Methods: Data from the population-based Northern Ireland BE register were matched to the Northern Ireland Cancer Registry for EAC outcomes until end 2013. Age-adjusted incidence of pediatric BE was calculated, and characteristics between pediatric and adult BE patients compared using Chi-square tests.

Results: Over 18 years, 42 pediatric BE patients (< 16 years) were identified, equivalent to an age-adjusted incidence of < 2 per 100,000 children. There was a clear age differential, with BE incidence increasing with age within the pediatric population. The majority (85.7%) of patients were male, a significantly higher male/female ratio than adult BE patients (p < 0.001). No pediatric BE patients progressed to high-grade dysplasia (HGD) or EAC, although the eldest patient was aged 34 years by the end of follow-up.

Conclusions: This is the largest series of pediatric BE ever reported. It demonstrates that pediatric BE is rare. The male preponderance of this condition is more apparent in childhood compared with adult cases. No children developed HGD/EAC during follow-up, suggesting that regular surveillance is not required, at least until adulthood.

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Source
http://dx.doi.org/10.1007/s10620-020-06462-5DOI Listing

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