• As a result of prolonged injury, the distal squamous epithelium is replaced with metaplastic columnar epithelium
  • It is the most important risk factor for oesophageal adenocarcinoma
  • It occurs in 10% of patients with GORD
  • Two criteria are required for a diagnosis of Barrett oesophagus;
    • Endoscopic evidence of columnar epithelial lining above the gastro-oesophageal junction
    • Histological evidence of intestinal metaplasia in the biopsy specimens from the columnar epithelium

 

  • The pathogenesis is unclear however re-epithelialisation by pluripotent stem cells in a low pH environment induced differentiation into gastric and intestinal type epithelium

 

Morphology

  • Gross – irregular circumferential band of red velvety mucosa at the gastro-oesophageal junction, with linear streaks or patches of similar mucosa in the distal oesophagus
  • Microsopic – intestinal type columnar epithelium (both with absorptive epithelial cells and mucin secreting oblet cells) interspersed with glandular gastric columnar mucosa
  • Epithelial cell dysplasia can arise in Barrett oesophagus

 

Clinical

  • Incidence is highest in white males, particularly between the ages of 40 to 60
  • Complications include ulceration with bleeding and stricture formation
  • Adenocarcinoma risk is increased 30 to 40 fold
 

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