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PMID: 1581911 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Persistent clonal areas and clonal expansion in Barrett's esophagus.

Cancer research ·Vol. 52 ·No. 10 ·1992-05-15 ·Pages 2946-50

Raskind WH, Norwood T, Levine DS, Haggitt RC, Rabinovitch PS, Reid BJ

Abstract

Three patients with Barrett's esophagus who had cytogenetic abnormalities detected in their metaplastic epithelium developed high-grade dysplasia or adenocarcinoma during prospective surveillance over a period of 1.5 to 6 years. In the 3 cases, cytogenetic abnormalities that were associated with the most advanced histological lesions were present in samples obtained 11, 25, and 48 months prior to the diagnosis of high-grade dysplasia or carcinoma. In a fourth patient, marker chromosomes found in a Barrett's adenocarcinoma were also present in an esophageal region spatially removed from the tumor. In all four patients, clonal cytogenetic abnormalities were present in samples obtained at widespread locations in the Barrett's segment. These observations suggest that in some patients with Barrett's esophagus clonal proliferations arise in regions of benign histology and spread to involve large areas of Barrett's mucosa. These clones persisted when the disease progressed to high-grade dysplasia or adenocarcinoma.

MeSH Terms
Adenocarcinoma/pathology Aged Barrett Esophagus/genetics,pathology Biopsy Clone Cells/pathology,physiology Cohort Studies Esophageal Neoplasms/pathology Flow Cytometry Follow-Up Studies Humans Karyotyping Male Metaplasia Middle Aged Prospective Studies
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Raskind W H
Department of Medicine, University of Washington School of Medicine, Seattle 98195.
Norwood T
Levine D S
Haggitt R C
Rabinovitch P S
Reid B J
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1992-05-15
Pages
2946-50
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NIDDK NIH HHS · P01 DK32971 · United States
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