2000
DOI: 10.1046/j.1440-1746.2000.02266.x
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Diagnostic criteria for gastrointestinal carcinomas in Japan and Western countries: Proposal for a new classification system of gastrointestinal epithelial neoplasia

Abstract: The intercountry differences in the diagnoses of adenoma/dysplasia and early carcinoma can, in large part, be resolved by adopting terminology based on neoplastic severity and depth of invasion. Problems with defining intramucosal invasion are thus avoided. Moreover, grouping high-grade adenoma/dysplasia and mucosal carcinoma together in one category is clinically useful, as patients with small mucosal neoplastic lesions can be cured by endoscopic local resection.

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Cited by 116 publications
(101 citation statements)
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“…Considerable discrepancies have been reported between diagnoses of colorectal epithelial neoplastic lesions made by Western and Japanese pathologists from endoscopic cold biopsies and resected specimens of the same lesions [1,2] . Japanese pathologists have distinguished five groups of lesions within the spectrum of colorectal epithelial neoplasia for cold biopsy specimens [Japanese Group Classification (JGC)], namely: normal or benign changes (inflammation/hyperplasia) without atypia [Group 1 (G1)]; non-neoplastic lesions with atypia resulting from inflammation, hyperplasia or regeneration [Group 2 (G2)]; neoplastic lesions with low-grade atypia, including adenomas with mild or moderate atypia and lesions difficult to diagnose as neoplastic or non-neoplastic [Group 3 (G3)]; neoplastic lesions strongly suspected of carcinoma, including adenomas with severe atypia [Group 4 (G4)]; and definite carcinoma [Group 5 (G5)], irrespective of intramucosal or submucosal invasion [3,4] .…”
Section: Introductionmentioning
confidence: 99%
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“…Considerable discrepancies have been reported between diagnoses of colorectal epithelial neoplastic lesions made by Western and Japanese pathologists from endoscopic cold biopsies and resected specimens of the same lesions [1,2] . Japanese pathologists have distinguished five groups of lesions within the spectrum of colorectal epithelial neoplasia for cold biopsy specimens [Japanese Group Classification (JGC)], namely: normal or benign changes (inflammation/hyperplasia) without atypia [Group 1 (G1)]; non-neoplastic lesions with atypia resulting from inflammation, hyperplasia or regeneration [Group 2 (G2)]; neoplastic lesions with low-grade atypia, including adenomas with mild or moderate atypia and lesions difficult to diagnose as neoplastic or non-neoplastic [Group 3 (G3)]; neoplastic lesions strongly suspected of carcinoma, including adenomas with severe atypia [Group 4 (G4)]; and definite carcinoma [Group 5 (G5)], irrespective of intramucosal or submucosal invasion [3,4] .…”
Section: Introductionmentioning
confidence: 99%
“…To overcome the differences between the conventional Western criteria and the JGC, the Vienna Classification attempted to combine the basic concepts of the conventional Western criteria, which emphasizes that invasion is an indicator of metastatic potential, with the strong points of the JGC, which values consistency between diagnoses of cold biopsy and resected specimens [2,9] . In the revised Vienna Classification (rVC), histopathologic diagnoses are classified into five categories according to neoplastic severity and depth of invasion.…”
Section: Introductionmentioning
confidence: 99%
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“…A number of previous studies have suggested that low-grade dysplasia (LGD) progresses to HGD [34][35][36][37], and that HGD becomes invasive GC within several months [38][39][40][41][42][43]. In 20-40 % of cases, diagnostic discrepancy between dysplasia evident at biopsy and GC observed in the resection specimen has been reported [34,37,44]. In most cases, the lesions were thought to be cancer at the time of initial biopsy [1,[44][45][46][47].…”
Section: Discussionmentioning
confidence: 99%
“…In 20-40 % of cases, diagnostic discrepancy between dysplasia evident at biopsy and GC observed in the resection specimen has been reported [34,37,44]. In most cases, the lesions were thought to be cancer at the time of initial biopsy [1,[44][45][46][47]. From a Western point of view, the final diagnosis rests on examination of the surgical or ESD specimen, because there is some possibility of cancer even if the diagnosis is LGD or HGD [21,23,36,[46][47][48].…”
Section: Discussionmentioning
confidence: 99%