Abstract:For patients with HGD, a lesion visible on endoscopy and/or HGD at multiple biopsy levels is associated with an increased risk for coexisting cancer. These patients should be considered for early esophagectomy.
“…Visible lesions in patients with dysplastic Barrett esophagus are associated with higher risk of invasive carcinoma (85,96) and should be treated with a tissueacquiring modality so these lesions can be appropriately resected and staged histologically (97).…”
“…Visible lesions in patients with dysplastic Barrett esophagus are associated with higher risk of invasive carcinoma (85,96) and should be treated with a tissueacquiring modality so these lesions can be appropriately resected and staged histologically (97).…”
“…Endoscopically visible lesions (Fig 1) associated with high-grade dysplasia have a higher risk for harboring cancer than fl at areas of dysplasia have. [16][17][18] Protruded, raised, or depressed lesions are at higher risk for submucosal invasion than fl at areas. Endoscopic resection (ER) provides an opportunity to accurately stage the depth of visible lesions in BE.…”
Section: Endoscopic Characteristics Of Bementioning
“…41,42 In a series of esophagectomies performed for presumed HGD identified by endoscopic biopsies, coexisting EA was found in 7 of 9 patients (78%) with a visible lesion and 7 of 22 patients (32%) without a visible lesion (P ϭ .02). 43 Risk of progression from HGD to EA is approximately 10% per year (range 6%-19%). Agreement: Aϩ 45%, A 40%, U 5%, D 6%, Dϩ 4%.…”
Section: Risk Of Progression To Esophageal Adenocarcinomamentioning
Diagnosis of Barrett’s oesophagus leads to an ongoing clinical uncertainty thereafter as to strategy for surveillance, due to the risk of dysplasia and carcinoma. The endoscopic findings have to be accurately classified macroscopically and on biopsy. Management of associated gastro-oesophageal reflux (GORD) is essential, and the chapter discusses detailed strategies for surveillance and treatment according to recent guidelines.
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