广州医药 ›› 2023, Vol. 54 ›› Issue (12): 44-48.DOI: 10.3969/j.issn.1000-8535.2023.12.007

• 论著 • 上一篇    下一篇

82例子宫内膜癌错配修复蛋白表达与临床病理特征的关系

吴克姣, 陈明光, 刘继英   

  1. 南平市第一医院病理科(福建南平 353000)
  • 收稿日期:2023-08-02 发布日期:2024-01-10

The structure and clinicopathological features of endometrial carcinoma in 82 cases

WU Kejiao, CHEN Mingguang, LIU Jiying   

  1. Department of Pathology,the First Hospital of Nanping City,Nanping 353000,China
  • Received:2023-08-02 Published:2024-01-10

摘要: 目的 探讨子宫内膜癌构成及临床病理特征。方法 以南平市第一医院2020年1月—2022年6月期间收治的82例子宫内膜癌患者为研究对象,收集其临床资料,通过免疫组织化学染色法检测4种错配修复蛋白表达,并分析错配修复蛋白表达与临床病理特征的关系。结果 82例患者中,70例(85.37%)为子宫内膜样癌,病理组织学类型以G1级30例(42.86%)为主,其他类型较为少见。错配修复蛋白表达总缺失率为35.71%,其中MUTL同源物1(MLH1)单独缺失率为2.86%,错配修复蛋白2抗体(MSH2)为4.29%,错配修复蛋白6抗体(MSH6)为14.29%,肿瘤错配修复基因PMS2抗体(PMS2)为14.29%;错配修复表达缺失(dMMR)组患者年龄50岁以上、伴脉管侵犯和淋巴结转移、组织学G3级和FIGO分期Ⅲ期占比高于错配修复表达正常(pMMR)组患者(P<0.05);MSH6蛋白表达缺失易发生在年龄50岁以上、有家族相关疾病史的患者(P<0.05);PMS2蛋白表达缺失易发生在组织学G2级、FIGO分期Ⅲ期、妊娠1次及以上、脉管内癌栓和淋巴结转移的患者(P<0.05)。结论 子宫内膜癌错配修复蛋白表达与其部分临床病理特征存在密切关联,可为患者后续治疗提供有价值的指导。

关键词: 子宫内膜癌, 临床病理特征, 免疫组织化学染色, 错配修复

Abstract: Objective To investigate the composition and clinicopathological features of endometrial carcinoma.Methods A total of 82 cases of endometrial carcinoma patients admitted to the First Hospital of Nanping City from January 2020 to June 2022 were studied.Epidemiological data were collected,and the expression of 4 mismatch repair proteins were detected by immunohistochemical staining,and their relationship with clinicopathological features was analyzed.Results Among 82 patients,70 cases(85.37%)were endometrioid carcinoma,and 30 cases(42.86%)were mainly G1 grade,other types were rare.The total deletion rate of mismatch repair proteins expression was 35.71%,in which MLH1 alone was 2.86%,MSH2 was 4.29%,MSH6 was14.29% and PMS2 was14.29%.The proportions of dMMR patients over 50 years old,with vascular invasion and lymph node metastasis,G3 grade histology and FIGO stage Ⅲ were significantly higher than those of the pMMR group(P<0.05).The loss of MSH6 protein expression was more likely to occur in patients over 50 years old with a family history of related diseases(P<0.05).The deletion of PMS2 protein expression was more likely to occur in patients with histological G2 grade,FIGO stage III,pregnancy of once or more and intravascular cancer thrombin and lymph node metastasis(P<0.05).Conclusions The expression of mismatch repair proteins in endometrial carcinoma is closely related to some clinicopathological features,which provides valuable guidance for follow-up treatment.

Key words: endometrial carcinoma, clinicopathological features, immunohistochemical staining, mismatch repair