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识别子宫内膜癌患者中的林奇综合征:形态学和临床方案的不足。

Identifying Lynch syndrome in patients with endometrial carcinoma: shortcomings of morphologic and clinical schemas.

机构信息

Department of Laboratory Medicine, University of Toronto, ON, Canada.

出版信息

Adv Anat Pathol. 2012 Jul;19(4):231-8. doi: 10.1097/PAP.0b013e31825c6b76.

Abstract

It has been suggested that reflex testing for Lynch syndrome (LS) using mismatch repair immunohistochemistry and/or microsatellite instability analysis in newly diagnosed colorectal carcinoma (CRC) patients is an emerging standard of care in the United States. The risk of gynecologic malignancy in women with LS approaches and even exceeds that of CRC. Furthermore, gynecologic malignancies are often the sentinel cancers in these patients. There is significant variation in practice, but some groups have similarly recommended deployment of reflex testing strategies in patients presenting with endometrial cancer (EC). The College of American Pathologists has stated that pathologists should recognize the histologic and clinical features that should prompt at least a recommendation for mismatch repair testing. Morphologic and clinical schemas in EC to identify microsatellite unstable/LS tumors are less refined than the colon-centric schemas (Amsterdam, Bethesda, and MsPath). Studies of LS EC are few and interpretation is limited by recruitment strategies and the myriad of definitions and study designs used. Although serous cell type is used to triage ovarian cancer patients for BRCA screening, cell type correlation in LS is less certain but seems to involve a spectrum of cell types. We review the morphologic and clinical features/schemas in LS EC and highlight limitations of restrictive aged-based screening strategies, uncertainty in current clinical schemas and equivocal results of morphologic studies of LS EC. With uncertainty of histologic and clinical schemas, and following developments in CRC, reflex testing of all/vast majority of newly diagnosed EC for LS should be considered.

摘要

有人认为,在新诊断的结直肠癌(CRC)患者中使用错配修复免疫组织化学和/或微卫星不稳定性分析进行林奇综合征(LS)的反射性检测,是美国新兴的护理标准。LS 女性的妇科恶性肿瘤风险接近甚至超过 CRC。此外,妇科恶性肿瘤通常是这些患者的首发癌症。尽管实践中存在很大差异,但一些团体同样建议在患有子宫内膜癌(EC)的患者中实施反射性检测策略。美国病理学家学院表示,病理学家应识别至少应建议进行错配修复检测的组织学和临床特征。识别微卫星不稳定/ LS 肿瘤的 EC 的形态学和临床方案不如以结肠为中心的方案(阿姆斯特丹、贝塞斯达和 MsPath)完善。LS EC 的研究较少,并且由于招募策略以及使用的无数定义和研究设计,解释受到限制。尽管浆液性细胞类型用于对卵巢癌患者进行 BRCA 筛查,但 LS 中的细胞类型相关性不太确定,但似乎涉及一系列细胞类型。我们回顾了 LS EC 的形态学和临床特征/方案,并强调了基于年龄的限制性筛查策略的局限性、当前临床方案的不确定性以及 LS EC 形态学研究的模棱两可结果。鉴于组织学和临床方案存在不确定性,并且在 CRC 之后,应考虑对所有/绝大多数新诊断的 EC 进行 LS 的反射性检测。

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