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本文引用的文献

1
The Barrett's Gland in Phenotype Space.表型空间中的巴雷特腺。
Cell Mol Gastroenterol Hepatol. 2014 Nov 12;1(1):41-54. doi: 10.1016/j.jcmgh.2014.10.001. eCollection 2015 Jan.
2
High Goblet Cell Count Is Inversely Associated with Ploidy Abnormalities and Risk of Adenocarcinoma in Barrett's Esophagus.高杯状细胞计数与巴雷特食管的倍体异常及腺癌风险呈负相关。
PLoS One. 2015 Jul 31;10(7):e0133403. doi: 10.1371/journal.pone.0133403. eCollection 2015.
3
Paired exome analysis of Barrett's esophagus and adenocarcinoma.巴雷特食管与腺癌的配对外显子组分析。
Nat Genet. 2015 Sep;47(9):1047-55. doi: 10.1038/ng.3343. Epub 2015 Jul 20.
4
The Presence of Genetic Mutations at Key Loci Predicts Progression to Esophageal Adenocarcinoma in Barrett's Esophagus.关键位点的基因突变预示巴雷特食管进展为食管腺癌。
Am J Gastroenterol. 2015 Jun;110(6):828-34. doi: 10.1038/ajg.2015.152. Epub 2015 May 26.
5
BOB CAT: A Large-Scale Review and Delphi Consensus for Management of Barrett's Esophagus With No Dysplasia, Indefinite for, or Low-Grade Dysplasia.BOB CAT:对无发育异常、发育异常不确定或低级别发育异常的巴雷特食管管理的大规模综述与德尔菲共识
Am J Gastroenterol. 2015 May;110(5):662-82; quiz 683. doi: 10.1038/ajg.2015.55. Epub 2015 Apr 14.
6
The use of molecular markers in predicting dysplasia and guiding treatment.分子标志物在预测发育异常和指导治疗中的应用。
Best Pract Res Clin Gastroenterol. 2015 Feb;29(1):113-24. doi: 10.1016/j.bpg.2014.11.003. Epub 2014 Nov 12.
7
Barrett oesophagus: lessons on its origins from the lesion itself.巴雷特食管:从病变本身了解其起源。
Nat Rev Gastroenterol Hepatol. 2015 Jan;12(1):50-60. doi: 10.1038/nrgastro.2014.181. Epub 2014 Nov 4.
8
Standardised reporting protocol for endoscopic resection for Barrett oesophagus associated neoplasia: expert consensus recommendations.巴雷特食管相关肿瘤内镜切除术的标准化报告方案:专家共识建议
Pathology. 2014 Oct;46(6):473-80. doi: 10.1097/PAT.0000000000000160.
9
Hedgehog signaling regulates FOXA2 in esophageal embryogenesis and Barrett's metaplasia.刺猬信号通路在食管胚胎发育和巴雷特化生过程中调节叉头框蛋白A2 。
J Clin Invest. 2014 Sep;124(9):3767-80. doi: 10.1172/JCI66603. Epub 2014 Aug 1.
10
Barrett's oesophagus patients with low-grade dysplasia can be accurately risk-stratified after histological review by an expert pathology panel.经专家病理小组进行组织学复查后,低度异型增生的 Barrett 食管患者可被准确地进行危险分层。
Gut. 2015 May;64(5):700-6. doi: 10.1136/gutjnl-2014-307278. Epub 2014 Jul 17.

巴雷特食管:病理学家的全面当代综述

Barrett's Esophagus: A Comprehensive and Contemporary Review for Pathologists.

作者信息

Naini Bita V, Souza Rhonda F, Odze Robert D

机构信息

*Department of Pathology & Lab Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA †Department of Medicine, University of Texas Southwestern Medical Center and the VA North Texas Health Care System ‡Esophageal Diseases Center, University of Texas Southwestern Medical Center and the VA North Texas Health Care System, Dallas, TX §Pathology Department, Brigham & Women's Hospital, Boston, MA.

出版信息

Am J Surg Pathol. 2016 May;40(5):e45-66. doi: 10.1097/PAS.0000000000000598.

DOI:10.1097/PAS.0000000000000598
PMID:26813745
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4833583/
Abstract

This review provides a summary of our current understanding of, and the controversies surrounding, the diagnosis, pathogenesis, histopathology, and molecular biology of Barrett's esophagus (BE) and associated neoplasia. BE is defined as columnar metaplasia of the esophagus. There is worldwide controversy regarding the diagnostic criteria of BE, mainly with regard to the requirement to histologically identify goblet cells in biopsies. Patients with BE are at increased risk for adenocarcinoma, which develops in a metaplasia-dysplasia-carcinoma sequence. Surveillance of patients with BE relies heavily on the presence and grade of dysplasia. However, there are significant pathologic limitations and diagnostic variability in evaluating dysplasia, particularly with regard to the more recently recognized unconventional variants. Identification of non-morphology-based biomarkers may help risk stratification of BE patients, and this is a subject of ongoing research. Because of recent achievements in endoscopic therapy, there has been a major shift in the treatment of BE patients with dysplasia or intramucosal cancer away from esophagectomy and toward endoscopic mucosal resection and ablation. The pathologic issues related to treatment and its complications are also discussed in this review article.

摘要

本综述总结了我们目前对巴雷特食管(BE)及其相关肿瘤的诊断、发病机制、组织病理学和分子生物学的理解以及围绕这些方面的争议。BE被定义为食管的柱状上皮化生。关于BE的诊断标准在全球范围内存在争议,主要涉及活检组织学鉴定杯状细胞的要求。BE患者患腺癌的风险增加,腺癌按照化生-发育异常-癌的顺序发展。对BE患者的监测很大程度上依赖于发育异常的存在和分级。然而,在评估发育异常方面存在显著的病理学局限性和诊断变异性,特别是对于最近才认识到的非传统变体。基于非形态学的生物标志物的鉴定可能有助于对BE患者进行风险分层,这是一个正在进行研究的课题。由于内镜治疗的最新进展,对于有发育异常或黏膜内癌的BE患者的治疗已发生重大转变,从食管切除术转向内镜黏膜切除术和消融术。本文还讨论了与治疗及其并发症相关的病理学问题。