具有腺肉瘤和癌混合特征的 SMARCA4/BRG1 缺陷子宫肿瘤:扩展SMARCA4驱动的妇科恶性肿瘤的分子形态谱。

IF 1.6 4区 医学 Q3 OBSTETRICS & GYNECOLOGY International Journal of Gynecological Pathology Pub Date : 2024-07-01 Epub Date: 2023-12-12 DOI:10.1097/PGP.0000000000000996
Christina H Wei, Evita Sadimin, Mark Agulnik, Susan E Yost, Teri A Longacre, Oluwole Fadare
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引用次数: 0

摘要

SMARCA4 基因编码 BRG1,BRG1 是 SWItch/蔗糖不发酵蛋白家族的成员,参与重要细胞过程的表观遗传转录调控。在子宫肌瘤中,SMARCA4/BRG1 缺乏症与一类新型未分化子宫肉瘤有关,这类肉瘤的特点是发病年龄较小、组织学为横纹肌样、局灶性蝶形结构、病理结果为高危、预后不良。在此,我们报告了一例34岁亚洲女性的SMARCA4/BRG1缺陷型子宫肿瘤病例,该病例符合未分化子宫肉瘤的临床病理特征。然而,该肿瘤表现出了几个以前从未强调过的独特特征,包括:(1)明显的栅栏状结构再现了传统的腺肉瘤;(2)横纹状肿瘤细胞形成索状和角蛋白阳性的内聚上皮岛;(3)与增生的其他部分共存一个空间上不同且离散的子宫内膜复合体非典型增生。通过免疫组化,肿瘤细胞的突触素呈弥漫性阳性,而 BRG1 则消失了。相关的分子研究结果包括SMARCA4基因的框移位突变,组蛋白修饰和染色质重塑基因(包括KMT2C、ARID1B、KAT6A和NCOR1)的突变,以及涉及APC和CTNNB1的Wnt信号转导基因突变。此外,还发现了MDM2和CDK4的拷贝数增殖。肿瘤突变负荷处于中等水平(6.8/MB),且微卫星稳定。综合来看,我们的病例在形态学和分子特征上与(1)未分化子宫肉瘤、(2)肉瘤过度生长的腺肉瘤以及(3)腺肉瘤和未分化子宫内膜癌混合瘤有重叠之处。这些混合特征进一步扩大了SMARCA4/BRG1缺陷型子宫肿瘤的分子形态谱。
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SMARCA4 / BRG1 -deficient Uterine Neoplasm With Hybrid Adenosarcoma and Carcinoma Features: Expanding the Molecular-morphologic Spectrum of SMARCA4 -driven Gynecologic Malignancies.

SMARCA4 gene encodes BRG1 , a member of the SWItch/sucrose non-fermentable protein family involved in epigenetic transcriptional regulation of important cellular processes. In the uterine corpus, SMARCA4 / BRG1 deficiency is associated with a novel class of undifferentiated uterine sarcomas, characterized by younger age onset, rhabdoid histology, focal phyllodiform architecture, high-risk pathologic findings, and dismal prognosis. Herein, we report a case of a 34-year-old Asian woman with a SMARCA4 / BRG1 -deficient uterine tumor fulfilling the clinicopathologic features of an undifferentiated uterine sarcoma. However, the tumor exhibited several unique features that have not been previously emphasized, including (1) conspicuous phyllodiform architecture recapitulating conventional adenosarcoma, (2) rhabdoid tumor cells forming cords and keratin-positive cohesive epithelial islands, and (3) cooccurrence with a spatially distinct and discrete endometrial complex atypical hyperplasia from the rest of the proliferation. By immunohistochemistry, the tumor cells were diffusely positive for synaptophysin, whereas BRG1 was lost. Pertinent molecular findings included frameshift mutations in the SMARCA4 gene, mutations in histone modification and chromatin remodeling genes, including KMT2C , ARID1B , KAT6A , and NCOR1 , and mutations in Wnt signaling involving APC and CTNNB1 . Copy number gain in MDM2 and CDK4 were also identified. The tumor mutation burden was intermediate (6.8/MB) and it was microsatellite stable. On balance, our case exhibited morphologic and molecular features that overlap with (1) an undifferentiated uterine sarcoma, (2) an adenosarcoma with sarcomatous overgrowth, and (3) a mixed adenosarcoma and undifferentiated endometrial carcinoma. These hybrid features further expand the molecular-morphologic spectrum of SMARCA4 / BRG1 -deficient uterine neoplasms.

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来源期刊
CiteScore
3.90
自引率
12.50%
发文量
154
审稿时长
6-12 weeks
期刊介绍: International Journal of Gynecological Pathology is the official journal of the International Society of Gynecological Pathologists (ISGyP), and provides complete and timely coverage of advances in the understanding and management of gynecological disease. Emphasis is placed on investigations in the field of anatomic pathology. Articles devoted to experimental or animal pathology clearly relevant to an understanding of human disease are published, as are pathological and clinicopathological studies and individual case reports that offer new insights.
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