The pathophysiology of Barrett's esophagus appears to be a sequential proce
ss; the squamous epithelium of the esophagus is replaced by multipotent und
ifferentiated cells: secondary to cellular damage in the course of gastroes
ophageal reflux disease these undifferentiated cells further differentiate
under the ongoing influence of mucosal damage, thus forming the typical mor
phology of Barrett mucosa. While the prevalence of gastroesophageal reflux
disease amounts to 10 % to 30 %, the prevalence of Barrett's esophagus is e
stimated to be 1 % in the general population. The epidemiologic data of Bar
rett's esophagus gain special attention with regard to the fact that the sp
ecialized columnar epithelium with intestinal metaplasia represents the onl
y recognized risk factor for the development of adenocarcinoma in the esoph
agus. Currently it is estimated that the risk of the development of an aden
ocarcinoma on the basis of Barrett's esophagus is about 30-50 fold higher t
han that in the general population.