Clinical, histological and receptor profiles of invasive breast cancer and ductal carcinoma in situ in females with germline pathogenic variants in PTEN and implications for germline testing.

IF 3.6 3区 医学 Q1 PATHOLOGY
Gelareh Farshid, S Jan Ibbetson, Malcolm Pradhan, Lachlan Henry, Nicholas David Manton, Andrew Dubowsky, Nicola Kazia Poplawski
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Abstract

PTEN hamartoma tumour syndrome (PHTS) is an autosomal dominant hereditary cancer syndrome, caused mostly by germline pathogenic variants in PTEN. Female carriers have an up to 80% lifetime risk of breast cancer. Pathological features of breast cancer in PHTS have seldom been reported. In a collaboration between all histopathology laboratories in our state and our statewide familial cancer service, we tracked the breast biopsies of 12 females with known PTEN pathogenic or likely pathogenic (P/LP) variants (January 1990 to January 2018). Two further cases were added by a Victorian cancer genetics unit. Breast cancer, inclusive of invasive cancer or ductal carcinoma in situ (DCIS), was diagnosed in 12 of 14 cases (85.7%). One case had a family history of PHTS, and six had a family history of breast cancer. The mean age at first breast cancer diagnosis was 41.6 years (range 27-63). Six cases developed more than one breast cancer. Five (42%) developed contralateral breast cancer. Ten of the 12 invasive cancers were of no special type, and two were reported as lobular carcinomas. None were grade 1. When reported, all cancers were hormone-receptor positive and HER2 negative. All were associated with DCIS. The DCIS spanned all grades. The two cases without breast cancer still required surgery for exuberant benign changes, including papillomas, fibroadenomatoid change, florid ductal epithelial hyperplasia, adenosis ​and stromal fibrosis. We note that the morphology and receptor profiles of breast cancer in individuals with P/LP PTEN variants are not distinctive. Contrary to prevalent beliefs, these cancers do not conform to the contemporary definition of apocrine breast carcinoma. Greater familiarity of healthcare professionals with the overall clinical and pathological findings in PHTS and the validated Cleveland Clinic PTEN calculator (http://www.lerner.ccf.org/gmi/ccscore) would improve the recognition of female PHTS individuals with breast cancer. Earlier identification of their cancer predisposition syndrome would benefit these patients and their families who are at high risk of a range of cancers.

PTEN种系致病变异女性浸润性乳腺癌和原位导管癌的临床、组织学和受体特征及其对种系检测的影响。
PTEN 仓瘤肿瘤综合征(PHTS)是一种常染色体显性遗传癌症综合征,主要由 PTEN 的种系致病变异引起。女性携带者一生中患乳腺癌的风险高达 80%。PHTS 乳腺癌的病理特征鲜有报道。在本州所有组织病理学实验室和全州家族性癌症服务机构的合作下,我们跟踪了12名已知PTEN致病或可能致病(P/LP)变异女性的乳腺活检病例(1990年1月至2018年1月)。维多利亚州癌症遗传学部门又增加了两个病例。14 例病例中有 12 例(85.7%)确诊为乳腺癌,包括浸润癌或导管原位癌(DCIS)。一个病例有 PHTS 家族史,六个病例有乳腺癌家族史。首次确诊乳腺癌的平均年龄为 41.6 岁(27-63 岁不等)。六例患者罹患一种以上的乳腺癌。5例(42%)罹患对侧乳腺癌。12 例浸润癌中有 10 例无特殊类型,有 2 例报告为小叶癌。没有 1 级癌症。所有报告的癌症均为激素受体阳性和 HER2 阴性。所有癌症都伴有 DCIS。DCIS跨越所有等级。两例未患乳腺癌的病例仍需进行手术治疗,以治疗乳头状瘤、纤维腺瘤样变、导管上皮增生、腺增生和基质纤维化等良性病变。我们注意到,P/LP PTEN 变体患者的乳腺癌形态和受体特征并无明显差异。与流行的观点相反,这些乳腺癌并不符合当代对无分泌乳腺癌的定义。医护人员若能进一步熟悉PHTS的整体临床和病理结果以及经过验证的克利夫兰诊所PTEN计算器(http://www.lerner.ccf.org/gmi/ccscore),就能更好地识别患有乳腺癌的女性PHTS患者。尽早发现她们的癌症易感综合征将使这些癌症高危患者及其家人受益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pathology
Pathology 医学-病理学
CiteScore
6.50
自引率
2.20%
发文量
459
审稿时长
54 days
期刊介绍: Published by Elsevier from 2016 Pathology is the official journal of the Royal College of Pathologists of Australasia (RCPA). It is committed to publishing peer-reviewed, original articles related to the science of pathology in its broadest sense, including anatomical pathology, chemical pathology and biochemistry, cytopathology, experimental pathology, forensic pathology and morbid anatomy, genetics, haematology, immunology and immunopathology, microbiology and molecular pathology.
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