首页> 外文期刊>American Journal of Surgical Pathology >Endometrial Carcinomas with a “Serous” Component in Young Women Are Enriched for DNA Mismatch Repair Deficiency, Lynch Syndrome, and POLE Exonuclease Domain Mutations
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Endometrial Carcinomas with a “Serous” Component in Young Women Are Enriched for DNA Mismatch Repair Deficiency, Lynch Syndrome, and POLE Exonuclease Domain Mutations

机译:具有“浆液”组件的子宫内膜癌,富集DNA错配修复缺乏,林奇综合征和杆外切核酸酶突变

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Supplemental Digital Content is available in the text. Endometrial carcinoma (EC), as described by Bokhman, has historically been classified as Type I (low-grade, hormone-dependant, young patients, good prognosis) or Type II (high-grade, hormone-independent, older patients, poor prognosis). This classification is no longer pragmatic, however, as EC is a much more heterogeneous disease. Four molecular subtypes of EC were identified by The Cancer Genome Atlas (TCGA), and subsequent studies have demonstrated its utility in predicting prognosis. While endometrial serous carcinoma (ESC), the prototypical Type II EC, largely occurs in older women, younger women with ESC were not accounted for in the Bokhman model and were underrepresented in the TCGA study. We hypothesized that a subset of ESCs in young patients do not represent bona fide serous carcinomas but rather high-grade endometrioid carcinomas mimicking a serous phenotype. We identified ESCs and mixed endometrioid/serous carcinomas in women <60 years (n=37), and analyzed their clinical, morphologic, immunohistochemical, and molecular characteristics. Sixteen percent showed mismatch repair deficiency (MMR-D) and 11% were diagnosed with Lynch syndrome. Additionally, 16% of cases tested harbored a hotspot POLE exonuclease domain mutation ( POLE- EDM). Morphologically, 47% of tumors showed confirmatory endometrioid features, including atypical hyperplasia, a low-grade endometrioid carcinoma component, or squamous differentiation. Clinically, the overall survival in patients with MMR-D and POLE -EDM was significantly better than that of patients without these features ( P =0.0329). In conclusion, ESCs in young patients comprise a heterogeneous group of tumors, demonstrating diverse clinical, immunohistochemical, morphologic, and molecular features which have implications for prognosis and adjuvant therapy.
机译:文本中提供了补充数字内容。如博赫曼所述的子宫内膜癌(EC),历史上被归类为I型(低级,激素依赖性,幼患者,良好预后)或II型(高档,激素独立,老年患者,预后不良)。然而,这种分类不再是务实的,因为EC是更加异质的疾病。通过癌症基因组地图集(​​TCGA)鉴定出四种EC的分子亚型,随后的研究表明其在预测预后的效用。虽然子宫内膜浆液癌(ESC),原型II欧共体主要发生在老年妇女中,但在博克曼模型中,ESC的年轻女性未占据,并且在TCGA研究中受到尊敬。我们假设年轻患者中的ESC子集不代表BONA FIDE浆液癌,而是高档的内疗中的癌模仿浆液表型。我们在女性<60岁(N = 37)中鉴定了ESC和混合的内疗中/浆液癌,分析了它们的临床,形态学,免疫组织化学和分子特性。 16%的百分比显示错配修复缺乏(MMR-D),11%被诊断出林奇综合征。此外,16%的案例测试了Harbored Hotspot杆外切核酸酶域突变(极针)。形态学上,47%的肿瘤显示出确认的子宫内膜特征,包括非典型增生,低级子宫内甲型癌组分或鳞状分化。临床上,MMR-D和杆状患者的整体存活率明显优于没有这些特征的患者(P = 0.0329)。总之,年轻患者的ESC包含一种异质肿瘤组,展示了具有对预后和佐剂治疗有影响的不同临床,免疫组织化学,形态学和分子特征。

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