Gastric or intestinal phenotypic expression in the carcinomas and background mucosa of multiple early gastric carcinomas

Citation
A. Kabashima et al., Gastric or intestinal phenotypic expression in the carcinomas and background mucosa of multiple early gastric carcinomas, HISTOPATHOL, 37(6), 2000, pp. 513-522
Citations number
37
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Journal title
HISTOPATHOLOGY
ISSN journal
03090167 → ACNP
Volume
37
Issue
6
Year of publication
2000
Pages
513 - 522
Database
ISI
SICI code
0309-0167(200012)37:6<513:GOIPEI>2.0.ZU;2-8
Abstract
Aims: The differences in phenotypic expression between multiple early gastr ic carcinomas (EGCs) and solitary EGCs were evaluated in this study. Methods and results: Fifty-three cases (53 lesions) of solitary EGCs and 50 cases (112 lesions) of multiple EGCs were studied. According to the classi fication of intestinal metaplasia, the phenotypes of carcinomas and backgro und mucosa were classified into four categories-complete intestinal type, i ncomplete intestinal type, gastric type and unclassified type-based on the combination of expression of CD10 (small intestinal brush border), MUC2 (in testinal goblet cell), HGM (gastric foveolar epithelium) and Con A (gastric pyloric glands), The incidence of gastric-type carcinomas (48%) and the in cidence of incomplete intestinal-type background mucosa (75%) among the mul tiple EGCs was higher than among the solitary EGCs. There was a significant difference in distribution of phenotypic expression of carcinomas and back ground mucosa between the solitary EGCs and the multiple EGCs, the latter b eing associated with incomplete intestinal metaplasia. Conclusions: Both the carcinomas and the background mucosa of multiple EGCs have an unstable status, since they more commonly possess the hybrid pheno type of the stomach and the small intestine than does solitary EGG. Such in stability is considered to contribute to a high neoplastic potential and th e multiple occurrence of carcinomas.