A. Csendes et al., ENDOSCOPIC ASSESSMENT OF THE PREVALENCE O F GASTRO ESOPHAGEAL JUNCTION INTESTINAL METAPLASIA IN GASTROESOPHAGEAL REFLUX, Revista Medica de Chile, 126(2), 1998, pp. 155-161
Background: The classic diagnosis of Barret esophagus is based on the
finding of three of more cm of distal esophagus covered by specialized
columnar epithelium. However, at the present time, it is based on the
presence of intestinal metaplasia in the junction of squamous-columna
r mucosae. Aim: To assess the prevalence of Barret esophagus using end
oscopic and pathological criteria in healthy subjects and in individua
ls with gastroesophageal reflux. Patients and methods: One hundred thi
rty nine controls and 372 patients with symptoms of gastroesophageal r
eflux subjected to an upper gastrointestinal endoscopy were studied. P
atients with Barret esophagus were classified as having a ''mini Barre
t: when the pathological presence of intestinal metaplasia was the onl
y finding. A ''short Barret esophagus'' was diagnosed when less than 3
cm were covered with fingerings of mucosal substitutions and ''extens
ive Barret esophagus'' when more than 3 cm of esophageal mucosa were s
ubstituted. Results: Two percent of controls, 12.4% of patients with g
astroesophageal reflux without esophagitis and 11.7% of such patients
with esophagitis had intestinal metaplasia in the gastroesophageal jun
ction. Patients with Barret esophagus were older than the rest of pati
ents. ''Short Barret esophagus'' is six times more frequent than ''ext
ensive Barret esophagus''. Esophageal erosions, peptic ulcers and sten
osis were more frequent in patients with extensive Barret esophagus. T
he prevalence of dysplasia was similar in all types of Barret esophagu
s. Conclusions: Intestinal metaplasia was very infrequent in control p
atients. In subjects with gastroesophageal reflux, classic endoscopic
diagnosis may miss up to 80% of patients with Barret esophagus. Thus,
gastroesophageal junction biopsies must be obtained in all patients wi
th symptoms of gastroesophageal reflux.