Fine-Needle Aspiration Is Suitable for Breast Cancer BRCA Molecular Assessment: A Case Report

F. Pepe, P. Pisapia, G. Russo, Mariantonia Nacchio, E. Vigliar, M. Giuliano, U. Malapelle, G. Troncone, Claudio Bellevicine
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Abstract

Breast cancer is the most common cause of cancer-related deaths in the female population worldwide. To the best of our knowledge, breast cancer (BRCA)1/2 gene mutations have not been described yet on breast cancer cytological specimens. Here we describe the case of a 38-year old woman with a family and personal history for breast cancer, who underwent a fine needle aspiration (FNA) procedure for a novel 30 mm lesion located in the external quadrants of the contralateral (left) breast. Cytological findings and ancillary immunostaining confirmed the diagnosis of a triple negative NST carcinoma. BRCA1/2 molecular assessment was carried out on DNA extracted from cytological (November 2020), biopsy (December 2014) and surgical resection (July 2015) specimens, as well as on the resection of a benign fibroadenoma, by using a next generation sequencing approach. Molecular analysis showed a pathogenic BRCA1 insertion (c.5266dupC; p.Q1756PfsTer74) in the cytological specimen (allelic fraction 92.0%), biopsy (allelic fraction 84.2%), surgical resection (allelic fraction 87.8%) and fibroadenoma (58.9%), demonstrating a germinal BRCA mutated status.
细针抽吸适用于乳腺癌BRCA分子评估:1例报告
乳腺癌是全球女性癌症相关死亡的最常见原因。据我们所知,乳腺癌(BRCA)1/2基因突变尚未在乳腺癌细胞学标本中被描述。在这里,我们描述了一个38岁的女性,她有乳腺癌的家族史和个人病史,她接受了细针抽吸(FNA)手术,治疗位于对侧(左)乳房外象限的一个30毫米的新病变。细胞学结果和辅助免疫染色证实了三阴性NST癌的诊断。采用下一代测序方法,对细胞学(2020年11月)、活检(2014年12月)和手术切除(2015年7月)标本中提取的DNA以及良性纤维腺瘤的切除进行BRCA1/2分子评估。分子分析显示一个致病性BRCA1插入(c.5266dupC;p.Q1756PfsTer74)在细胞学标本(等位基因分数92.0%)、活检(等位基因分数84.2%)、手术切除(等位基因分数87.8%)和纤维腺瘤(58.9%)中均存在,表明BRCA突变状态。
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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