INTRODUCTION:
Barrett esophagussometimes calledBarrett
syndromeorcolumnar epithelium lined lower
oesophagus(CELLO), refers to an abnormal change
(metaplasia) in the cells of the lower portion of
theesophagus.
When the normalsquamous epitheliumlining of the
esophagus is replaced bygoblet cells(cells usually found
lower in the gastrointestinal tract), Barrett's esophagus is
diagnosed.
The medical significance of Barrett esophagus is its strong
association with esophagealadenocarcinoma, a particularly
lethal cancer.
SIGNS AND SYMPTOMS:
The change from normal to premalignant cells that indicate Barrett
esophagus does not cause any particular symptoms.
Barrett esophagus, however, is associated with the following symptoms:
frequent and longstandingheartburn
trouble swallowing (dysphagia)
vomiting blood (hematemesis)
pain under the breastbone where the esophagus meets the stomach
unintentional weight loss because eating is painful
The risk of developing Barrett esophagus is increased bycentral
obesity(vs. peripheral obesity).
MECHANISM
Barrett esophagus occurs due to chronic inflammation.
The principal cause of the chronic inflammation is GERD.
In this disease, acidic stomach, bile, small intestine and
pancreatic contents cause damage to the cells of the lower
esophagus.
Recently, it was shown thatbile acidsare able to induce
intestinal differentiation, in gastroesophageal junction cells,
through inhibition of theEpidermal growth factor receptor
(EGFR) receptor and theprotein kinaseenzymeAkt.
DIAGNOSIS:
Diagnosis of Barrett esophagus requiresendoscopy (more
specifically,esophagogastroduodenoscopy, a procedure in which a
fibre optic cable is inserted through the mouth to examine the
esophagus, stomach, andduodenum) andbiopsy.
Barrett esophagus is marked by the presence ofcolumnar
epitheliain the lower esophagus, replacing the normalsquamous
cellepithelium—an example ofmetaplasia
The cells of Barrett esophagus, after biopsy, are classified into four
general categories:
1.non-dysplastic
2.low-gradedysplasia
3.high-grade dysplasia
4.frankcarcinoma
5.High-grade dysplasia
MANAGEMENT:
Treatment options for high-grade dysplasia include:
-surgical removal of the esophagus (esophagectomy)
-endoscopic treatments such asendoscopic mucosal resectionor
radiofrequency ablation (destruction).
Proton pump inhibitor drugs have not yet been proven to prevent
esophageal cancer.
Laser treatmentis used in severe dysplasia, while overt malignancy may
requiresurgery,radiation therapy, or systemicchemotherapy.
Endoscopic mucosal resection(EMR) has also been evaluated as a
management technique.Additionally an operation known as aNissen
fundoplicationcan reduce the reflux of acid from the stomach into the
esophagus.
In a variety of studies, non-steroidal anti-inflammatory drugs (NSAIDS),
likeaspirin, have shown evidence of preventing esophageal cancer in
Barrett esophagus patients.