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Are ulcers a marker for invasive carcinoma in barrett's esophagus? data from a diagnostic variability study with clinical follow-up

dc.contributor.authorMontgomery, Elizabethen_US
dc.contributor.authorBronner, Mary P.en_US
dc.contributor.authorGreenson, Joel K.en_US
dc.contributor.authorHaber, Marian M.en_US
dc.contributor.authorHart, Johnen_US
dc.contributor.authorLamps, Laura W.en_US
dc.contributor.authorLauwers, Gregory Y.en_US
dc.contributor.authorLazenby, Audrey J.en_US
dc.contributor.authorLewin, David N.en_US
dc.contributor.authorRobert, Marie E.en_US
dc.contributor.authorWashington, Kayen_US
dc.contributor.authorGoldblum, John R.en_US
dc.date.accessioned2010-06-01T22:09:58Z
dc.date.available2010-06-01T22:09:58Z
dc.date.issued2002-01en_US
dc.identifier.citationMontgomery, Elizabeth; Bronner, Mary P . ; Greenson, Joel K . ; Haber, Marian M . ; Hart, John; Lamps, Laura W . ; Lauwers, Gregory Y . ; Lazenby, Audrey J . ; Lewin, David N . ; Robert, Marie E . ; Washington, Kay; Goldblum, John R . (2002). "Are ulcers a marker for invasive carcinoma in barrett's esophagus? data from a diagnostic variability study with clinical follow-up." The American Journal of Gastroenterology 97(1): 27-31. <http://hdl.handle.net/2027.42/75186>en_US
dc.identifier.issn0002-9270en_US
dc.identifier.issn1572-0241en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/75186
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11808966&dopt=citationen_US
dc.description.abstractWe correlated follow-up information from 138 patients with Barrett's esophagus and varying degrees of dysplasia with the presence of ulcers. Methods A group of pathologist participants were asked to contribute patients’ initial biopsy slides showing Barrett's esophagus (BE) without dysplasia and with epithelial changes indefinite for dysplasia, low grade dysplasia (LGD), high grade dysplasia (HGD), and adenocarcinoma. From the initial 250 cases used for a diagnostic reproducibility study, follow-up information was available for 138 patients. Results There were 44 cases submitted as BE, 22 as BE with epithelial changes indefinite for dysplasia, 26 as BE with LGD, 33 as BE with HGD, and 13 as BE with adenocarcinoma. Ulcers were present in 35/138 cases (25%), including 3/44 cases of BE without dysplasia (7%), 2/22 cases of BE with epithelial changes indefinite for dysplasia (9%), 0/26 cases of BE with LGD (0%), 10/33 cases of BE with HGD (30%), and 7/13 cases of BE with adenocarcinoma (54%). On follow-up, there were no invasive carcinomas detected among the BE without dysplasia group (median follow-up = 38.5 months). Adenocarcinomas were detected in 4/22 cases (18%) submitted as BE with epithelial changes indefinite for dysplasia at 19, 55, 60, and 62 months and in 4/26 cases (15%) of BE with LGD at 9, 9, 11, and 60 months. None of these carcinomas occurred in cases in which an ulcer was present in the initial biopsy specimen. Among the 33 HGD cases, 20 (60%) were found to have adenocarcinoma on subsequent resection specimens. The presence of an ulcer with HGD increased the likelihood of finding carcinoma in the resection specimen, as 8/10 biopsies (80%) of HGD patients with ulcers had carcinoma, compared to 12/23 biopsies (52%) of HGD patients without ulcers. All of the cases interpreted as adenocarcinomas on biopsy were found either to have invasive carcinoma on esophageal resection or to have metastases that were demonstrated in unresectable patients. Conclusion If an ulcer accompanies HGD in a biopsy specimen from a patient with BE, it is likely that invasive carcinoma is also present at that time.en_US
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dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
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dc.publisherBlackwell Publishing Ltden_US
dc.rights2002 by Am. Coll. of Gastroenterologyen_US
dc.titleAre ulcers a marker for invasive carcinoma in barrett's esophagus? data from a diagnostic variability study with clinical follow-upen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, The Johns Hopkins University, Baltimore, Maryland, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Washington, Seattle, Washington, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, MCP Hahnemann University, Philadelphia, Pennsylvania, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Chicago, Chicago, Illinois, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Arkansas, Fayetteville, Arkansas, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Alabama, Birmingham, Alabama, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, Medical University of South Carolina, Charleston, South Carolina, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, Yale University, New Haven, Connecticut, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, Vanderbilt University, Nashville, Tennessee, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, Cleveland Clinic Foundation, Cleveland, Ohio, USAen_US
dc.identifier.pmid11808966en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/75186/1/j.1572-0241.2002.05420.x.pdf
dc.identifier.doi10.1111/j.1572-0241.2002.05420.xen_US
dc.identifier.sourceThe American Journal of Gastroenterologyen_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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