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与种系突变相关的恶性布伦纳瘤

Malignant Brenner tumor associated with a germline mutation.

作者信息

Toboni Michael D, Smith Haller J, Dilley Sarah E, Novak Lea, Leath Charles A

机构信息

University of Alabama at Birmingham, Department of Obstetrics & Gynecology, United States.

University of Alabama at Birmingham, Division of Gynecologic Oncology, United States.

出版信息

Gynecol Oncol Rep. 2017 May 31;21:17-19. doi: 10.1016/j.gore.2017.05.006. eCollection 2017 Aug.

DOI:10.1016/j.gore.2017.05.006
PMID:28616458
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5458647/
Abstract

•The first woman with a Malignant Brenner tumor and a mutation is described.•Not all women with epithelial ovarian cancers are referred for genetic counseling.•Women should be referred for genetics regardless of how rare the histology.

摘要

•描述了首例患有恶性布伦纳瘤且存在一种突变的女性。

•并非所有上皮性卵巢癌女性都会被转诊进行遗传咨询。

•无论组织学类型多么罕见,女性都应被转诊进行遗传学评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40f3/5458647/adc9013932e5/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40f3/5458647/29938c763610/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40f3/5458647/5be3d4543648/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40f3/5458647/adc9013932e5/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40f3/5458647/29938c763610/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40f3/5458647/5be3d4543648/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40f3/5458647/adc9013932e5/gr3.jpg

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引用本文的文献

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A report of twenty cases of ovarian Brenner tumor and literature review: a case series study.二十例卵巢 Brenner 肿瘤报告及文献复习:病例系列研究。
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Malignant Brenner Tumor of the Ovary: A Systematic Review of the Literature.卵巢恶性勃勒纳瘤:文献系统综述
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Brenner Tumor of the Ovary: A 10-Year Single Institution Experience and Comprehensive Review of the Literature.卵巢 Brenner 肿瘤:10 年单机构经验及文献全面复习。

本文引用的文献

1
Germline and somatic testing for ovarian Cancer: An SGO clinical practice statement.卵巢癌的种系和体细胞检测:SGO 临床实践声明。
Gynecol Oncol. 2024 Feb;181:170-178. doi: 10.1016/j.ygyno.2023.12.010. Epub 2024 Jan 12.
2
Large, Prospective Analysis of the Reasons Patients Do Not Pursue BRCA Genetic Testing Following Genetic Counseling.对基因咨询后患者不进行BRCA基因检测原因的大型前瞻性分析。
J Genet Couns. 2017 Aug;26(4):859-865. doi: 10.1007/s10897-016-0064-5. Epub 2017 Jan 16.
3
Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.
Med Sci (Basel). 2023 Feb 7;11(1):18. doi: 10.3390/medsci11010018.
遗传/家族性高风险评估:乳腺和卵巢,第 2.2015 版。
J Natl Compr Canc Netw. 2016 Feb;14(2):153-62. doi: 10.6004/jnccn.2016.0018.
4
Nonserous Ovarian Epithelial Tumors.非浆液性卵巢上皮性肿瘤
Surg Pathol Clin. 2011 Mar;4(1):397-459. doi: 10.1016/j.path.2010.12.012. Epub 2011 Feb 22.
5
Inherited Mutations in Women With Ovarian Carcinoma.遗传性突变与卵巢癌女性。
JAMA Oncol. 2016 Apr;2(4):482-90. doi: 10.1001/jamaoncol.2015.5495.
6
Germline BRCA1/2 testing practices in ovarian cancer: Current state and opportunities for new directions.BRCA1/2 种系检测在卵巢癌中的应用:现状与新方向的机遇。
Gynecol Oncol. 2016 Jan;140(1):90-4. doi: 10.1016/j.ygyno.2015.10.010. Epub 2015 Oct 22.
7
Adherence patterns to National Comprehensive Cancer Network (NCCN) guidelines for referral to cancer genetic professionals.遵循美国国立综合癌症网络(NCCN)关于转诊至癌症遗传专业人员的指南的模式。
Gynecol Oncol. 2015 Jul;138(1):109-14. doi: 10.1016/j.ygyno.2015.04.029. Epub 2015 Apr 28.
8
Ovarian Brenner tumour: a morphologic and immunohistochemical analysis suggesting an origin from fallopian tube epithelium.卵巢 Brenner 肿瘤:形态学和免疫组织化学分析提示来源于输卵管上皮。
Eur J Cancer. 2013 Dec;49(18):3839-49. doi: 10.1016/j.ejca.2013.08.011. Epub 2013 Sep 5.
9
Tamoxifen and risk of contralateral breast cancer for BRCA1 and BRCA2 mutation carriers.他莫昔芬和 BRCA1/2 基因突变携带者对侧乳腺癌风险。
J Clin Oncol. 2013 Sep 1;31(25):3091-9. doi: 10.1200/JCO.2012.47.8313. Epub 2013 Aug 5.
10
Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer.胚系 BRCA 突变与前列腺癌中淋巴结受累、远处转移和不良生存结局的风险增加相关。
J Clin Oncol. 2013 May 10;31(14):1748-57. doi: 10.1200/JCO.2012.43.1882. Epub 2013 Apr 8.