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基因决定的卵巢癌的组织病理学特征。

Histopathologic features of genetically determined ovarian cancer.

作者信息

Shaw P A, McLaughlin J R, Zweemer R P, Narod S A, Risch H, Verheijen R H M, Ryan A, Menko F H, Kenemans P, Jacobs I J

机构信息

Department of Pathology, University Health Network, University of Toronto, ON, Canada.

出版信息

Int J Gynecol Pathol. 2002 Oct;21(4):407-11. doi: 10.1097/00004347-200210000-00011.

Abstract

Inheritance of germline mutations of BRCA1 or BRCA2 genes account for approximately 10% of ovarian carcinomas, but the characterization of these genetically determined cancers is incomplete. The objective of our study was to characterize the histologic features of ovarian carcinomas associated with germline mutations of BRCA1 and BRCA2. Thirty-two ovarian carcinomas associated with germline BRCA1 or BRCA2 mutations and 40 ovarian carcinomas from patients screened as negative for germline mutations were obtained from three centers. A gynecologic pathologist, blinded to mutation status, reviewed each case, with documentation of the histologic type, Gynecologic Oncology Group (GOG) grade, architectural and nuclear grade, Silverberg grade, and mitotic activity. All BRCA1 and BRCA2 mutation-associated cases were invasive serous carcinomas, and of these 50% were GOG grade 3, 41% had an architectural grade of 3 (predominant solid architecture), 84% a nuclear grade of 3, 72% a mitotic score of 3 (>25 mitoses per 10 HPF), and 75% a Silverberg grade of 3. The differences in histologic type (p = 0.001) and Silverberg grade (p = 0.002) between these tumors and the control group were statistically significant and remained so when comparisons between BRCA carriers and noncarriers were restricted to carcinomas of serous histology alone. Ovarian carcinomas associated with germline mutations of BRCA1/BRCA2 are, in this study, invasive serous carcinomas, with a statistically significant higher histologic grade than ovarian carcinomas without BRCA mutations when using the recently proposed Silverberg grading system.

摘要

BRCA1或BRCA2基因种系突变导致的卵巢癌约占卵巢癌总数的10%,但这些基因决定型癌症的特征描述并不完整。我们研究的目的是描述与BRCA1和BRCA2种系突变相关的卵巢癌的组织学特征。从三个中心获取了32例与BRCA1或BRCA2种系突变相关的卵巢癌以及40例经筛查种系突变为阴性的患者的卵巢癌。一名对突变状态不知情的妇科病理学家对每个病例进行了检查,并记录了组织学类型、妇科肿瘤学组(GOG)分级、结构和核分级、西尔弗伯格分级以及有丝分裂活性。所有与BRCA1和BRCA2突变相关的病例均为浸润性浆液性癌,其中50%为GOG 3级,41%的结构分级为3级(主要为实性结构),84%的核分级为3级,72%的有丝分裂评分为3级(每10个高倍视野中有超过25个有丝分裂),75%的西尔弗伯格分级为3级。这些肿瘤与对照组在组织学类型(p = 0.001)和西尔弗伯格分级(p = 0.002)上的差异具有统计学意义,当仅将BRCA携带者与非携带者之间的比较限制在浆液性组织学的癌症时,这种差异仍然存在。在本研究中,与BRCA1/BRCA2种系突变相关的卵巢癌为浸润性浆液性癌,使用最近提出的西尔弗伯格分级系统时,其组织学分级在统计学上显著高于无BRCA突变的卵巢癌。

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