Literature DB >> 30234520

Refined Criteria for Separating Low-grade Dysplasia and Nondysplastic Barrett Esophagus Reduce Equivocal Diagnoses and Improve Prediction of Patient Outcome: A 10-Year Review.

Kevin M Waters1, Kevan J Salimian2, Lysandra Voltaggio2, Elizabeth A Montgomery2.   

Abstract

The indefinite for dysplasia (IFD) category in Barrett esophagus (BE) is used for biopsies that are neither unequivocally dysplastic nor negative for dysplasia (NFD). In 2012, we refined our criteria so that BE with maintained cell polarity and surface gastric-type mucin vacuoles is considered NFD even with mild to moderate nuclear enlargement. A total of 1549 cases from 1130 patients with BE biopsies were identified from 2007 to 2016. Follow-up on patients with IFD biopsies was obtained to learn if the new thresholds better defined risk of progression. The earlier cases (2007-2011) were less likely than later cases (2012-2016) to be NFD (84.0% vs. 90.4%) and more likely to be IFD (8.4% vs. 4.3%). The proportions of low-grade dysplasia (3.9% vs. 2.5%, high-grade dysplasia (1.4% vs. 1.3%), and intramucosal carcinoma (2.3% vs. 1.6%) were similar between the earlier and later cases, respectively. Later IFD cases were more frequently dysplastic (3/21, 14.3%) on the next biopsy than earlier cases (1/48, 2.1%). The rate of dysplasia on the next biopsy for NFD cases was not higher in the later cases (6/222, 2.7%) than the earlier cases (16/360, 4.4%). Improved diagnostic criteria reduced the proportion of IFD cases by nearly 50% from 2007 to 2016. This change coincided with a higher proportion of IFD cases having dysplasia on the next biopsy. NFD patients had no increase in dysplasia on the next biopsy providing evidence that dysplastic cases are not missed by the refined criteria.

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Year:  2018        PMID: 30234520     DOI: 10.1097/PAS.0000000000001162

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  5 in total

Review 1.  Inflammatory bowel disease- and Barrett's esophagus-associated neoplasia: the old, the new, and the persistent struggles.

Authors:  Dipti M Karamchandani; Qin Zhang; Xiao-Yan Liao; Jing-Hong Xu; Xiu-Li Liu
Journal:  Gastroenterol Rep (Oxf)       Date:  2019-08-13

2.  Extremely well-differentiated adenocarcinoma of the stomach: diagnostic pitfalls in endoscopic biopsy.

Authors:  Jongwon Lee; In-Seob Lee; Ji Yong Ahn; Young Soo Park; Jihun Kim
Journal:  J Pathol Transl Med       Date:  2021-11-16

Review 3.  Utility of ancillary studies in the diagnosis and risk assessment of Barrett's esophagus and dysplasia.

Authors:  Won-Tak Choi; Gregory Y Lauwers; Elizabeth A Montgomery
Journal:  Mod Pathol       Date:  2022-03-08       Impact factor: 8.209

4.  Cell polarity (the 'four lines') distinguishes gastric dysplasia from epithelial changes in reactive gastropathy.

Authors:  Kevin M Waters; Kevan J Salimian; Naziheh Assarzadegan; Danielle Hutchings; Elias P Makhoul; Annika L Windon; Mary T Wong; Lysandra Voltaggio; Elizabeth A Montgomery
Journal:  Histopathology       Date:  2020-10-14       Impact factor: 7.778

5.  The utility of P53 immunohistochemistry in the diagnosis of Barrett's oesophagus with indefinite for dysplasia.

Authors:  Wladyslaw Januszewicz; Nastazja D Pilonis; Tarek Sawas; Richard Phillips; Maria O'Donovan; Ahmad Miremadi; Shalini Malhotra; Monika Tripathi; Adrienn Blasko; David A Katzka; Rebecca C Fitzgerald; Massimiliano di Pietro
Journal:  Histopathology       Date:  2022-06       Impact factor: 7.778

  5 in total

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