Barrett’s Esophagus (BE)
(Gastroenterol 2006;131:1392-99 & 2005;128:1468-70. Am J. Gastroenterol 2002;97:1888-95)
DEFINITION:
Barrett’s esophagus (BE) is displacement of the squamocolumnar junction (SCJ) proximally to the gastroesophageal junction (GEJ) and intestinal metaplasia (IM)
Intestinal metaplasia is histologically characterized by acid mucin-containing goblet cells using H & E alcian blue (pH 2.5) stain
BE is of little importance if not for the well established association with adenocarcinoma (AC) of the esophagus (BE is a premalignant condition)
Note: The endoscopic Prague C & M Criteria (first presented in Prague in 9/2004) has recently been proposed as a standard way of accurately recognizing and grading BE
This classification may likely replace the standard ‘Short’ or ‘Long’ segment terminology
EPIDEMIOLOGY:
Short segment BE is found 10-15% and Long segment BE is found in 3-7% of symptomatic GERD patients undergoing endoscopy
IM of cardia (not BE) can be found in as much as 6-35% of patients undergoing endoscopy for any reason
Prevalence increases with age, suggesting an acquired condition; Unlike BE it is found equally in ♂ & ♀ and whites & blacks
Reports of up to 25% of BE patients are under the age of 50 – not just an “old person’s disease” (Am J Gastroenterol 2006;101:2187-93)
ETIOLOGIES:
Risk factors:
Acquired disorder: Age and Duration of reflux (<1 year of symptoms: 4% prevalence; >10 years of symptoms: 21% prevalence)
Men > Women; Ethnicity (Caucasian > African American); Obesity; Average age at diagnosis: 63
PATHOPHYSIOLOGY:
Acquired condition resulting from severe esophageal mucosal injury; Unclear why some GERD patients get BE and others do not
Most BE patients have larger hiatal hernias and lower basal LES pressures (as compared to those with esophagitis or those without reflux)
Cyclooxygenase (COX)-2 is involved in chronic inflammation and may be increased by exposure to acid; Possible chemoprevention role in future
Evolution of BE [Intestinal metaplasia (IM)] to cancer: Negative for dysplasia » Indefinite for dysplasia » Low-grade dysplasia (LGD) » High-grade dysplasia (HGD) » Adenocarcinoma (AC)
Time course variable and most never progress to dysplasia
Progression not preordained (i.e. some can go from HGD back to intestinal metaplasia)
LABORATORY STUDIES: