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子宫体的条索状和玻璃样变子宫内膜样腺癌(CHEC)以CTNNB1突变为特征,可显示不良临床结局。

Corded and Hyalinized Endometrioid Adenocarcinoma (CHEC) of the Uterine Corpus are Characterized by CTNNB1 Mutations and Can Show Adverse Clinical Outcomes.

作者信息

Ladwig Nicholas R, Umetsu Sarah E, Zaloudek Charles, Rabban Joseph, Garg Karuna

机构信息

Department of Pathology, University of California, San Francisco, CA.

出版信息

Int J Gynecol Pathol. 2021 Mar 1;40(2):103-115. doi: 10.1097/PGP.0000000000000671.

Abstract

Corded and hyalinized endometrioid adenocarcinoma (CHEC) is a morphologic variant of endometrioid adenocarcinoma that is typically low-grade [International Federation of Gynecology and Obstetrics (FIGO) grade 1-2]. CHEC exhibits a biphasic appearance with gland forming adenocarcinoma merging with a diffuse component with corded growth often in a hyalinized matrix; squamous differentiation is frequent and osteoid production can be seen. This morphologic appearance can invoke a large differential diagnosis including carcinosarcoma. CHEC is thought to be associated with good clinical outcome although the available data is sparse. We performed detailed clinical, morphologic, immunohistochemical, and molecular analyses on a cohort of 7 CHEC. Six cases exhibited features of classic low-grade CHEC while one case showed greater cytologic atypia (high-grade CHEC). Patient age ranged from 19 to 69 yr. Four patients presented at stage I, 2 at stage II, and 1 at stage III. All tumors demonstrated nuclear staining for beta-catenin and loss of E-cadherin in the corded and hyalinized component. There was relative loss of epithelial markers. Loss of PTEN and ARID1A was seen in 4 and 3 tumors, respectively, and 1 tumor displayed loss of MLH1 and PMS2. Next-generation sequencing revealed CTNNB1 and PI3K pathway mutations in all 7 cases with TP53 and RB1 alterations in the high-grade CHEC. Clinical follow-up was available for 6 patients; 2 died of disease (48 and 50 mo), 2 are alive with disease (both recurred at 13 mo), and 2 have no evidence of disease (13 and 77 mo). Our study shows that CHEC universally harbors CTNNB1 mutations with nuclear staining for beta-catenin, can rarely show high-grade cytology, and can be associated with adverse clinical outcomes.

摘要

条索状及玻璃样变的子宫内膜样腺癌(CHEC)是子宫内膜样腺癌的一种形态学变异型,通常为低级别(国际妇产科联盟(FIGO)1-2级)。CHEC呈现双相外观,腺管形成的腺癌与弥漫成分融合,弥漫成分常呈条索状生长于玻璃样变基质中;鳞状分化常见,可见类骨质生成。这种形态学表现可引发包括癌肉瘤在内的多种鉴别诊断。尽管现有数据较少,但CHEC被认为与良好的临床预后相关。我们对7例CHEC病例进行了详细的临床、形态学、免疫组化及分子分析。6例表现为典型的低级别CHEC特征,而1例显示出更大的细胞异型性(高级别CHEC)。患者年龄范围为19至69岁。4例患者为I期,2例为II期,1例为III期。所有肿瘤在条索状及玻璃样变成分中均显示β-连环蛋白核染色及E-钙黏蛋白缺失。上皮标志物相对缺失。4例和3例肿瘤分别出现PTEN和ARID1A缺失,1例肿瘤显示MLH1和PMS2缺失。二代测序显示所有7例均有CTNNB1和PI3K通路突变,高级别CHEC中有TP53和RB1改变。6例患者有临床随访资料;2例死于疾病(分别为48个月和50个月),2例带瘤生存(均在13个月时复发),2例无疾病证据(分别为13个月和77个月)。我们的研究表明,CHEC普遍存在CTNNB1突变且有β-连环蛋白核染色,很少表现为高级别细胞学特征,且可能与不良临床预后相关。

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