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本文引用的文献

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Diagnosis and management of Barrett esophagus: European Society of Gastrointestinal Endoscopy (ESGE) Guideline.巴雷特食管的诊断和管理:欧洲胃肠道内镜学会(ESGE)指南。
Endoscopy. 2023 Dec;55(12):1124-1146. doi: 10.1055/a-2176-2440. Epub 2023 Oct 9.
2
Diagnosis and Management of Barrett's Esophagus: An Updated ACG Guideline. Barrett 食管的诊断和管理:ACG 指南更新。
Am J Gastroenterol. 2022 Apr 1;117(4):559-587. doi: 10.14309/ajg.0000000000001680.
3
Identification of Prognostic Phenotypes of Esophageal Adenocarcinoma in 2 Independent Cohorts.在 2 个独立队列中鉴定食管腺癌的预后表型。
Gastroenterology. 2018 Dec;155(6):1720-1728.e4. doi: 10.1053/j.gastro.2018.08.036. Epub 2018 Aug 27.
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Histology of Barrett's Metaplasia: Do Goblet Cells Matter?巴雷特化生的组织学:杯状细胞重要吗?
Dig Dis Sci. 2018 Aug;63(8):2042-2051. doi: 10.1007/s10620-018-5151-z.
5
Factors Associated With Progression of Barrett's Esophagus: A Systematic Review and Meta-analysis.与 Barrett 食管进展相关的因素:系统评价和荟萃分析。
Clin Gastroenterol Hepatol. 2018 Jul;16(7):1046-1055.e8. doi: 10.1016/j.cgh.2017.11.044. Epub 2017 Dec 2.
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Integrated genomic characterization of oesophageal carcinoma.食管癌的综合基因组特征分析
Nature. 2017 Jan 12;541(7636):169-175. doi: 10.1038/nature20805. Epub 2017 Jan 4.
7
Length of Barrett's oesophagus and cancer risk: implications from a large sample of patients with early oesophageal adenocarcinoma.巴雷特食管长度与癌症风险:来自一大群早期食管腺癌患者的启示。
Gut. 2016 Feb;65(2):196-201. doi: 10.1136/gutjnl-2015-309220. Epub 2015 Jun 25.
8
Australian clinical practice guidelines for the diagnosis and management of Barrett's esophagus and early esophageal adenocarcinoma.澳大利亚巴雷特食管和早期食管腺癌诊断与管理临床实践指南。
J Gastroenterol Hepatol. 2015 May;30(5):804-20. doi: 10.1111/jgh.12913.
9
Does the Incidence of Adenocarcinoma of the Esophagus and Gastric Cardia Continue to Rise in the Twenty-First Century?—a SEER Database Analysis.21世纪食管腺癌和贲门腺癌的发病率仍在上升吗?——一项监测、流行病学和最终结果(SEER)数据库分析
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10
British Society of Gastroenterology guidelines on the diagnosis and management of Barrett's oesophagus.英国胃肠病学会 Barrett 食管诊断和管理指南。
Gut. 2014 Jan;63(1):7-42. doi: 10.1136/gutjnl-2013-305372. Epub 2013 Oct 28.

食管及食管胃交界腺癌发生前Barrett食管的检测

Detection of Barrett's Esophagus Prior to Development of Esophageal and Esophagogastric Junction Adenocarcinoma.

作者信息

Russin Michelle, Harbrecht Matthew, Mishra Ankit, Peddu Dhiraj, Kubina Matthew, Chang Joy W, Burns Jennifer A, Arasim Maria E, Rubenstein Joel H

机构信息

Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan.

Division of Gastroenterology, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan.

出版信息

Clin Gastroenterol Hepatol. 2025 Apr 30. doi: 10.1016/j.cgh.2025.02.016.

DOI:10.1016/j.cgh.2025.02.016
PMID:40315974
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12353451/
Abstract

BACKGROUND & AIMS: Guidelines differ on the definition of Barrett's esophagus (BE). We aimed to estimate the detection rate of esophagogastroduodenoscopy (EGD) with biopsy for BE, using longitudinal outcome of adenocarcinoma of the esophagus or esophagogastric junction (EAC, EGJAC) as the gold standard.

METHODS

We performed retrospective analyses of US Veterans with EAC/EGJAC between 2017 and 2021 who had an EGD before cancer diagnosis. We reviewed a random sample of 200 cases of EAC and 100 cases of EGJAC to tabulate the detection rate of EGD with biopsy, stratified by Siewert classification (S1 or S2).

RESULTS

After manual review, there were 136 S1 and 108 S2 cases. Among patients with endoscopic suspicion of BE who had biopsies, 96.8% of S1 and 97.9% of S2 had intestinal metaplasia (IM). BE defined as ≥1 cm with IM had a detection rate of 66.2% for S1 and 39.8% for S2. When restricted to EGDs with appropriate biopsies, the detection rate of ≥1 cm with IM improved to 70.3% in S1 and 41.4% in S2. Seventy-three percent of S1 cases and 90% of S2 cases without BE diagnosed were related to lack of endoscopic suspicion for BE. BE or a visible lesion was present in 70% of photographs from EGDs not suspected of having BE by the original endoscopist.

CONCLUSIONS

IM seems required for development of EAC and likely EGJAC. EGD with biopsy had only modest rate for detecting a precursor state for subsequent adenocarcinoma and was lower for S2 compared with S1. Variability in endoscopic suspicion, including segments <1 cm, are potential areas for improvement in detection of BE by EGD.

摘要

背景与目的

巴雷特食管(BE)的定义在不同指南中存在差异。我们旨在以食管或食管胃交界腺癌(EAC、EGJAC)的纵向结局作为金标准,评估经活检的食管胃十二指肠镜检查(EGD)对BE的检出率。

方法

我们对2017年至2021年间患有EAC/EGJAC且在癌症诊断前接受过EGD检查的美国退伍军人进行了回顾性分析。我们回顾了200例EAC和100例EGJAC的随机样本,以列出经活检的EGD的检出率,并按Siewert分类(S1或S2)进行分层。

结果

经人工审核,有136例S1病例和108例S2病例。在内镜检查怀疑有BE并进行活检的患者中,96.8%的S1病例和97.9%的S2病例有肠化生(IM)。定义为≥1 cm且有IM的BE在S1中的检出率为66.2%,在S2中的检出率为39.8%。当仅限于进行了适当活检的EGD时,≥1 cm且有IM的检出率在S1中提高到70.3%,在S2中提高到41.4%。73%的S1病例和90%的未诊断为BE的S2病例与内镜未怀疑有BE有关。在最初的内镜医师未怀疑有BE的EGD照片中,70%存在BE或可见病变。

结论

IM似乎是EAC以及可能的EGJAC发生所必需的。经活检的EGD对后续腺癌前驱状态的检出率仅为中等水平,且S2的检出率低于S1。内镜怀疑的变异性,包括<1 cm的节段,是通过EGD检测BE时潜在的可改进领域。