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[一项基于人群的研究中,通过免疫组织化学检测高级别异型增生腺瘤中错配修复蛋白核表达改变的患病率及其相关风险特征]

[Prevalence of altered mismatch repair protein nuclear expression detected by immunohistochemistry on adenomas with high-grade dysplasia and features associated with this risk in a population-based study].

作者信息

Basterra Marta, Gomez Marta, Mercado María Del Rosario, Irisarri Rebeca, Amorena Edurne, Arrospide Arantzazu, Montes Marta, Aisa Gregorio, Cambra Koldo Iñaki, Urman Jesús

机构信息

Servicio de Aparato Digestivo, Complejo Hospitalario de Navarra, Pamplona, España.

Servicio de Aparato Digestivo, Complejo Hospitalario de Navarra, Pamplona, España.

出版信息

Gastroenterol Hepatol. 2016 Oct;39(8):500-7. doi: 10.1016/j.gastrohep.2015.10.008. Epub 2016 Jan 12.

Abstract

INTRODUCTION

Alteration of mismatch repair system protein expression detected by immunohistochemistry (IHQ) in tumoural tissue is a useful technique for Lynch Syndrome (LS) screening. A recent review proposes LS screening through immunohistochemical study not only in all diagnosed cases of colorectal cancer (CRC) but also in advanced adenomas, especially in young patients.

OBJECTIVE

To assess the prevalence of altered IHQ carried out in all adenomas with high-grade dysplasia (HGD) diagnosed in our community in 2011, as well as the variables associated with this alteration.

METHODS

We included all the cases of adenomatous polyps with HGD diagnosed in the three public pathology laboratories of Navarre during 2011 and performed a statistical study to assess the association between different patient and lesion characteristics and altered IHQ results.

RESULTS

A total of 213 colonic adenomas with HGD were diagnosed, and 26 (12.2%) cases were excluded from the final analysis (2 known LS, 22 without IHQ study and 2 with inconclusive IHQ studies). The final number of adenomas included was 187. Pathologic results were found in 10 cases (5.35%)-6 cases in MLH1 and PMS2, 2 cases in PMS2, 1 case in MSH6 and 1 case in MSH2 and MSH6. The factors showing a statistically significant association with the presence of abnormal proteins were the synchronous presence of CRC, the presence of only one advanced adenoma, proximal location of HGD and age <50 years.

CONCLUSIONS

The percentage of pathologic nuclear expression found in IHQ is high. Consequently, screening of all diagnosed HGD could be indicated, especially in young patients, with a single AA and proximal HGD.

摘要

引言

通过免疫组织化学(IHQ)检测肿瘤组织中错配修复系统蛋白表达的改变是林奇综合征(LS)筛查的一项有用技术。最近的一项综述建议,不仅要对所有确诊的结直肠癌(CRC)病例,而且要对晚期腺瘤,特别是年轻患者,进行免疫组织化学研究以筛查LS。

目的

评估2011年在我们社区诊断的所有高级别异型增生(HGD)腺瘤中IHQ改变的患病率,以及与这种改变相关的变量。

方法

我们纳入了2011年在纳瓦拉的三个公共病理实验室诊断的所有HGD腺瘤性息肉病例,并进行了一项统计研究,以评估不同患者和病变特征与IHQ结果改变之间的关联。

结果

共诊断出213例HGD结肠腺瘤,26例(12.2%)病例被排除在最终分析之外(2例已知LS,22例未进行IHQ研究,2例IHQ研究结果不确定)。纳入的腺瘤最终数量为187例。在10例(5.35%)病例中发现病理结果——6例MLH1和PMS2异常,2例PMS2异常,1例MSH6异常,1例MSH2和MSH6异常。与异常蛋白存在具有统计学显著关联的因素是同时存在CRC、仅存在一个晚期腺瘤、HGD的近端位置以及年龄<50岁。

结论

IHQ中发现的病理性核表达百分比很高。因此,可能需要对所有确诊的HGD进行筛查,特别是对年轻患者、单发高级别腺瘤和近端HGD患者。

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