Suppr超能文献

结合免疫组织化学和分子方法诊断非典型息肉样腺肌瘤的进展:病例报告及文献综述

Advances in the Diagnosis of Atypical Polypoid Adenomyoma Combining Immunohistochemical and Molecular-Based Approaches: Case Report and Review of the Literature.

作者信息

Azúa-Romeo Francisco Javier, Bayona-Morón Sonia, Rodriguez-Perez Irene, Angulo-Biedma Bárbara

机构信息

Department of Pathology, Analiza, 28001 Madrid, Spain.

Department of Anatomy and Histology, Faculty of Medicine, University of Zaragoza, 50009 Zaragoza, Spain.

出版信息

Curr Issues Mol Biol. 2024 Dec 17;46(12):14204-14214. doi: 10.3390/cimb46120850.

Abstract

Atypical polypoid adenomyoma (APA) is a benign uterine lesion with a premalignant potential and occurs in women of reproductive age. The histological pattern is characterized by irregular epithelial proliferation and muscular stroma. Based on a case report, we performed a systematic review of the literature to assess the main immunohistochemical and molecular markers that contribute to its differential diagnosis against endometrial adenocarcinoma (EC). The distinction is essential for offering to patients a conservative treatment compared to the radical management required for endometrial cancer, a critical issue for the significant physical and psychological consequences that one procedure or another can have on women's health. We performed a meta-analysis of the immunohistochemical markers used for the histological diagnosis of APA, comparing it with our case study. The evaluated markers were beta-catenin, h-caldesmon, desmin, vimentin, smooth muscle alpha-actin, CD10, Ki67, estrogen receptor (ER), progesterone receptor (PR), pan-cytokeratin, PTEN, PMS2, MSH2, MSH6, p53, MLH1, and p16. Discrepancies were observed in the expression of CD10, h- caldesmon, and p16 when comparing APA with EC. The results of the case evaluated by our team showed beta-catenin nuclear expression and positive immunostaining for pan-cytokeratin, ER, and PR in the glands; smooth muscle actin and desmin positive expression in stromal muscle; and p16 positive immunostaining in squamous morules. Moreover, the c.94G>T p. (Asp132Tyr) mutation in the gene was detected. This study supports the combination of appropriate immunohistochemical and molecular markers, along with the presumptive histological diagnosis, and determines the correct classification of the lesion as APA and not as other malignant pathologies, allowing for the establishment of a treatment protocol adjusted to the biological reality of this pathology.

摘要

非典型息肉样腺肌瘤(APA)是一种具有恶变潜能的良性子宫病变,发生于育龄期女性。其组织学模式以不规则上皮增生和肌性间质为特征。基于一例病例报告,我们对文献进行了系统综述,以评估有助于其与子宫内膜腺癌(EC)进行鉴别诊断的主要免疫组化和分子标志物。这种区分对于为患者提供保守治疗至关重要,因为与子宫内膜癌所需的根治性治疗相比,这是一个关键问题,因为一种治疗方法或另一种治疗方法可能对女性健康产生重大的身体和心理影响。我们对用于APA组织学诊断的免疫组化标志物进行了荟萃分析,并与我们的病例研究进行了比较。评估的标志物包括β-连环蛋白、h-钙调蛋白、结蛋白、波形蛋白、平滑肌α-肌动蛋白、CD10、Ki67、雌激素受体(ER)、孕激素受体(PR)、全细胞角蛋白、PTEN、PMS2、MSH2、MSH6、p53、MLH1和p16。在将APA与EC进行比较时,观察到CD10、h-钙调蛋白和p16表达存在差异。我们团队评估的病例结果显示,腺体中β-连环蛋白核表达以及全细胞角蛋白、ER和PR免疫染色阳性;间质肌中平滑肌肌动蛋白和结蛋白表达阳性;鳞状小体中p16免疫染色阳性。此外,还检测到该基因中的c.94G>T p.(Asp132Tyr)突变。本研究支持将适当的免疫组化和分子标志物与推测的组织学诊断相结合,并确定病变正确分类为APA而非其他恶性病变,从而能够制定适合该病变生物学特性的治疗方案。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验