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首页> 外文期刊>Cancer epidemiology, biomarkers and prevention: A publication of the American Association for Cancer Research >Familiality in Barrett's esophagus, adenocarcinoma of the esophagus, and adenocarcinoma of the gastroesophageal junction.
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Familiality in Barrett's esophagus, adenocarcinoma of the esophagus, and adenocarcinoma of the gastroesophageal junction.

机译:巴雷特食管,食道腺癌和胃食管交界处腺癌的家族性。

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BACKGROUND AND AIM: The familial aggregation of Barrett's esophagus, adenocarcinoma of the esophagus, and adenocarcinoma of the gastroesophageal junction, jointly termed familial Barrett's esophagus, may represent a complex genetic trait. The aim of this study was to determine the proportion of patients with these diseases who have familial Barrett's esophagus. METHODS: Information on gastroesophageal reflux symptoms, known risk factors for Barrett's esophagus, and family history of Barrett's esophagus and cancers, was collected at six hospitals using a structured questionnaire from probands with either long-segment Barrett's esophagus, adenocarcinoma of the esophagus, or adenocarcinoma of the gastroesophageal junction. Family history of Barrett's esophagus or esophageal cancer in a first- or second-degree relative was determined by reviewing medical records of all relatives reported to be affected. RESULTS: Seventy one of 411 (17.3%) probands reported an affected first- and/or second-degree relative. Upon review of medical records of the reportedly affected relatives, familial Barrett's esophagus was definitively determined in the case of 30 (7.3%) probands comprising 17 of 276 (6.2%) with Barrett's esophagus, 11 of 116 (9.5%) with adenocarcinoma of the esophagus, and 2 of 21 (9.5%) with adenocarcinoma of the gastroesophageal junction. The diagnosis in the relative reported by the proband to be affected was found not to be Barrett's esophagus or adenocarcinoma in 15 (3.6%) cases. The diagnosis could not be determined in 26 (6.3%) cases in which the proband reported an affected relative. There were no significant differences in age of disease onset, gender, race, or gastroesophageal reflux symptoms between definitive familial Barrett's esophagus probands and nonfamilial probands. CONCLUSION: Familial Barrett's esophagus can be confirmed in 7.3% of persons presenting with Barrett's esophagus, adenocarcinoma of the esophagus, or adenocarcinoma of the gastroesophageal junction.
机译:背景与目的:Barrett食道,食道腺癌和胃食管交界处的腺癌的家族聚集,合称为家族性Barrett食道,可能代表着复杂的遗传特征。这项研究的目的是确定患有家族性巴雷特食管的这些疾病患者的比例。方法:在六家医院中,采用结构化问卷从患有长节段巴雷特食管,食道腺癌或腺癌的先证者收集有关胃食管反流症状,巴雷特食管的已知危险因素以及巴雷特食管和癌症的家族史的信息。胃食管连接处。一级或二级亲属的巴雷特食管或食道癌的家族病史是通过查阅所有据报告受影响的亲戚的病历来确定的。结果:411名先证者中的71名(17.3%)报告了一级和/或二级亲戚受到影响。在对据报道受影响的亲属的病历进行审查后,确定了家族性Barrett食道,其中30例(7.3%)先证者占276例中的17例(6.2%)为Barrett食道,116例中有11例(9.5%)为腺癌。食道,其中21例中有2例(9.5%)伴有胃食管交界处的腺癌。先证者报告受影响的亲属的诊断在15例(3.6%)病例中发现不是Barrett食道或腺癌。在先证者报告患病亲属的26例(6.3%)病例中,无法确定诊断。明确的家族性巴雷特食管先证者和非家族性先证者的发病年龄,性别,种族或胃食管反流症状没有显着差异。结论:7.3%出现Barrett食道,食道腺癌或胃食管交界处腺癌的患者中,可以确认家族性Barrett食道。

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