Limited value of type III intestinal metaplasia in predicting risk of gastnrc carcinoma
Journal of Clinical Pathology, ISSN: 0021-9746, Vol: 40, Issue: 11, Page: 1287-1290
1987
- 64Citations
- 11Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations64
- Citation Indexes61
- 61
- CrossRef47
- Clinical Citations2
- PubMed Guidelines2
- Policy Citations1
- Policy Citation1
- Captures11
- Readers11
- 11
Article Description
Endoscopic gastric biopsy specimens taken in 1976 from 174 patients were reviewed. Biopsy specimens from 44 patients showed intestinal metaplasia, and subtyping by mucin histochemistry showed that 16 were of type I, 14 of type II, and 14 of type III. Only two of these 174 patients developed gastric adenocarcinoma over the next 10 to 11 years: one with type II and one with type III intestinal metaplasia. Case notes of a separate group of 68 patients with gastric adenocarcinoma diagnosed in 1985 were reviewed for evidence of intestinal metaplasia in a previous gastric biopsy. Only two patients had previously been biopsied; one of these biopsy specimens showed type II intestinal metaplasia and the other showed no intestinal metaplasia. These findings suggest that subtyping of intestinal metaplasia in endoscopic gastric biopsy specimens is of only limited value in identifying patients at risk of gastric adenocarcinoma who require long term follow up.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0023607856&origin=inward; http://dx.doi.org/10.1136/jcp.40.11.1287; http://www.ncbi.nlm.nih.gov/pubmed/3693566; https://jcp.bmj.com/lookup/doi/10.1136/jcp.40.11.1287; https://dx.doi.org/10.1136/jcp.40.11.1287; https://jcp.bmj.com/content/40/11/1287
BMJ
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