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巴雷特食管发育异常。

Dysplasia in Barrett esophagus.

作者信息

Lao Christopher D, Simmons Melanie, Syngal Sapna, Bresalier Robert S, Fortlage Laurie, Normolle Daniel, Griffith Kent A, Appelman Henry D, Brenner Dean E

机构信息

Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michigan 48109, USA.

出版信息

Cancer. 2004 Apr 15;100(8):1622-7. doi: 10.1002/cncr.20149.

DOI:10.1002/cncr.20149
PMID:15073848
Abstract

BACKGROUND

Dysplasia in Barrett esophagus is a premalignant condition that is associated with an increased risk of developing esophageal adenocarcinoma. Unfortunately, clinical investigation aimed at prevention of progression to malignant disease has been hampered by the variable prevalence of dysplasia reported in the literature. The objective of the current study was to more accurately determine the prevalence of dysplasia among individuals with Barrett esophagus who would be available for enrollment in a chemoprevention trial.

METHODS

The pathology archives of 3 institutions were reviewed over a 5-year period for all reports of diagnoses of Barrett esophagus. Surgical cases, malignancies, and duplicate or referral cases were excluded from the analysis.

RESULTS

A total of 790 cases of Barrett esophagus were identified. Of these, 37 (4.7%) were cases of low-grade dysplasia (LGD), and 20 (2.5%) were cases of high-grade dysplasia. The University of Michigan Medical Center (Ann Arbor, MI) diagnosed 18 cases of LGD, Henry Ford Hospital (Detroit, MI) diagnosed 15 cases of LGD, and Brigham and Women's Hospital (Boston, MA) diagnosed 4 cases of LGD in patients with Barrett esophagus over the 5-year study period.

CONCLUSIONS

The confirmed low prevalence of cases of LGD will affect the design of future clinical trials of chemopreventive interventions for Barrett esophagus.

摘要

背景

巴雷特食管发育异常是一种癌前病变,与食管腺癌发生风险增加相关。遗憾的是,针对预防进展为恶性疾病的临床研究因文献报道的发育异常患病率存在差异而受到阻碍。本研究的目的是更准确地确定可纳入化学预防试验的巴雷特食管患者中发育异常的患病率。

方法

回顾了3家机构5年期间所有巴雷特食管诊断报告的病理档案。分析排除了手术病例、恶性肿瘤以及重复或转诊病例。

结果

共识别出790例巴雷特食管病例。其中,37例(4.7%)为低级别发育异常(LGD),20例(2.5%)为高级别发育异常。在5年研究期间,密歇根大学医学中心(密歇根州安娜堡)诊断出18例LGD,亨利·福特医院(密歇根州底特律)诊断出15例LGD,布莱根妇女医院(马萨诸塞州波士顿)诊断出4例巴雷特食管患者的LGD。

结论

确诊的LGD病例低患病率将影响未来巴雷特食管化学预防干预临床试验的设计。

相似文献

1
Dysplasia in Barrett esophagus.巴雷特食管发育异常。
Cancer. 2004 Apr 15;100(8):1622-7. doi: 10.1002/cncr.20149.
2
Dysplasia as a predictive marker for invasive carcinoma in Barrett esophagus: a follow-up study based on 138 cases from a diagnostic variability study.发育异常作为巴雷特食管浸润癌的预测标志物:一项基于诊断变异性研究中138例病例的随访研究
Hum Pathol. 2001 Apr;32(4):379-88. doi: 10.1053/hupa.2001.23511.
3
Clinical and endoscopic factors predict higher pathologic grades of Barrett dysplasia.临床和内镜因素可预测巴雷特异型增生的更高病理分级。
Cancer. 2007 Feb 15;109(4):668-74. doi: 10.1002/cncr.22451.
4
Low-grade dysplasia in Barrett's esophagus has a high risk of progression.巴雷特食管的低级别发育异常有很高的进展风险。
Endoscopy. 2007 Jul;39(7):581-7. doi: 10.1055/s-2007-966592.
5
Extent of low-grade dysplasia is a risk factor for the development of esophageal adenocarcinoma in Barrett's esophagus.低度异型增生的程度是巴雷特食管发生食管腺癌的一个危险因素。
Am J Gastroenterol. 2007 Mar;102(3):483-93; quiz 694. doi: 10.1111/j.1572-0241.2007.01073.x.
6
Dysplasia and cancer in a large multicenter cohort of patients with Barrett's esophagus.巴雷特食管患者大型多中心队列中的发育异常和癌症
Clin Gastroenterol Hepatol. 2006 May;4(5):566-72. doi: 10.1016/j.cgh.2006.03.001. Epub 2006 Apr 17.
7
DNA abnormalities as marker of risk for progression of Barrett's esophagus to adenocarcinoma: image cytometric DNA analysis in formalin-fixed tissues.DNA异常作为巴雷特食管进展为腺癌风险的标志物:福尔马林固定组织的图像细胞计量DNA分析
Am J Gastroenterol. 2004 Oct;99(10):1887-94. doi: 10.1111/j.1572-0241.2004.30886.x.
8
Advanced pathology under squamous epithelium on initial EMR specimens in patients with Barrett's esophagus and high-grade dysplasia or intramucosal carcinoma: implications for surveillance and endotherapy management.巴雷特食管合并高级别异型增生或黏膜内癌患者初次内镜黏膜切除术标本中鳞状上皮下的高级病理学表现:对监测和内镜治疗管理的意义
Gastrointest Endosc. 2009 Sep;70(3):417-21. doi: 10.1016/j.gie.2009.01.047. Epub 2009 Jun 24.
9
Dysplasia and risk of further neoplastic progression in a regional Veterans Administration Barrett's cohort.一个地区退伍军人管理局巴雷特食管队列中的发育异常及进一步肿瘤进展风险
Am J Gastroenterol. 2005 Apr;100(4):775-83. doi: 10.1111/j.1572-0241.2005.41300.x.
10
Aneuploidy and overexpression of Ki67 and p53 as markers for neoplastic progression in Barrett's esophagus: a case-control study.非整倍体以及Ki67和p53的过表达作为巴雷特食管肿瘤进展的标志物:一项病例对照研究。
Am J Gastroenterol. 2009 Nov;104(11):2673-80. doi: 10.1038/ajg.2009.437. Epub 2009 Jul 28.

引用本文的文献

1
Prevalence of Barrett's Esophagus in Asian Countries: A Systematic Review and Meta-analysis.亚洲国家巴雷特食管的患病率:一项系统评价和荟萃分析。
Clin Gastroenterol Hepatol. 2015 Nov;13(11):1907-18. doi: 10.1016/j.cgh.2015.07.050. Epub 2015 Aug 7.
2
Ki-67 Antigen Overexpression Is Associated with the Metaplasia-Adenocarcinoma Sequence in Barrett's Esophagus.Ki-67 抗原过表达与 Barrett 食管的化生-腺癌序列相关。
Gastroenterol Res Pract. 2012;2012:639748. doi: 10.1155/2012/639748. Epub 2012 Jul 11.
3
Endoscopic treatments for Barrett's esophagus: a systematic review of safety and effectiveness compared to esophagectomy.
内镜治疗 Barrett 食管:与食管切除术相比的安全性和有效性的系统评价。
BMC Gastroenterol. 2010 Sep 27;10:111. doi: 10.1186/1471-230X-10-111.
4
Large intra- and inter-individual variability of genes expression levels limits potential predictive value of molecular diagnosis of dysplasia in Barrett's esophagus.基因表达水平在个体内和个体间存在较大差异,这限制了巴雷特食管发育异常分子诊断的潜在预测价值。
J Mol Med (Berl). 2008 Feb;86(2):233-42. doi: 10.1007/s00109-007-0271-5. Epub 2007 Oct 19.