Foveolar type dysplasia in Barrett esophagus
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Brown, Ian S
Whiteman, David C
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CitationBrown, Ian S, David C Whiteman, and Gregory Y Lauwers. 2010. “Foveolar Type Dysplasia in Barrett Esophagus.” Modern Pathology 23 (6) (March 12): 834–843. doi:10.1038/modpathol.2010.59.
AbstractAdenocarcinoma of the lower esophagus and esophagogastric junction is increasing in incidence in Western countries. A metaplasia (Barrett esophagus)—dysplasia—carcinoma sequence induced by gastroesophageal reflux disease is established. Two patterns of Barrett dysplasias have been described—adenomatous (type 1) and non-adenomatous (type 2 or foveolar/hyperplastic type). Interestingly, little is known about non-adenomatous dysplasia. Esophagogastrectomy cases from 41 patients with glandular dysplasia with and without associated invasive adenocarcinoma of the lower esophagus were evaluated for expression of MUC2, MUC5AC, CDX2, villin, Ki67 and p53. Results were correlated with sub-classification of the dysplasia into morphologic patterns of adenomatous vs foveolar vs hybrid type. In addition, clinicopathological parameters including the presence and extent of background intestinal metaplasia were also evaluated. Foveolar type dysplasia was present in 46% of the cases and thus, was more common than adenomatous type or hybrid type (both ~27%) dysplasia. Immunohistochemistry confirmed the histological stratification in all cases. Foveolar type dysplasia commonly expressed MUC5AC (P<0.12) but was consistently negative for markers of intestinal differentiation, MUC2, CDX2 and villin (all P<0.01). By contrast, adenomatous type dysplasia frequently displayed intestinal differentiation markers (all P<0.0001) Hybrid-type dysplasia was similar to adenomatous type dysplasia in showing expression of intestinal differentiation markers (P<0.01) and therefore could not be sustained as a separate category. In conclusion, our study provides evidence for a non intestinal pathway to neoplastic development in Barrett esophagus, that is, gastric metaplasia—foveolar dysplasia—adenocarcinoma.
Citable link to this pagehttp://nrs.harvard.edu/urn-3:HUL.InstRepos:35140973
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