基因检测对年轻乳腺纤维腺瘤患者的意义

S. Mikhailova, V. V. Semenova, T. V. Nasedkina, T. T. Valiev, D. Khestanov, S. Varfolomeeva
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引用次数: 0

摘要

导言纤维腺瘤是儿童和青少年乳腺中最常见的良性肿瘤。在某些情况下,它们可能是遗传性肿瘤易感综合征的一部分,与终生罹患恶性肿瘤的高风险相关,因此基因检测具有重要意义。本研究的目的是根据新一代测序(NGS)的结果,描述乳腺纤维腺瘤年轻患者癌症相关基因的基因突变谱。本研究招募了 16 名患有乳腺纤维腺瘤的少女,她们在 2020 年至 2023 年期间接受了儿科肿瘤学和血液学研究所的随访。研究人员通过 NGS 进行了基因检测。4例(25%)患者发现了癌症相关基因的致病变异。其中两例患者的乳腺纤维腺瘤是与 PTEN 失活相关的考登综合征的一部分;两例患者携带 BRCA1 和 BRCA2 基因的致病变异。对患有乳腺纤维腺瘤的年轻患者进行基因检测对于优化治疗策略以降低高危人群的癌症风险非常重要。
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The relevance of genetic testing in young patients with breast fibroadenomas
Introduction. Fibroadenomas are the most common benign tumors of the mammary glands in children and adolescents. In some cases, they may be part of hereditary tumor predisposition syndromes associated with a high risk of developing malignant neoplasms throughout life, and therefore genetic testing is relevant.The purpose of the study is to discribe the spectrum of genetic mutations in cancer-associated genes according to the results of next generation sequencing (NGS) in young patients with breast fibroadenomas.Matherials and methods. Sixteen teenage girls with fibroadenomas of the breast who were followed up in Research Institute of Pediatric Oncology and Hematology from 2020 to 2023 were enrolled in this study. Genetic testing by NGS was performed.Results. Pathogenic variants in cancer-associated genes were found in 4 (25 %) patients. In two cases, fibroadenomas were a part of Cowden’s syndrome associated with PTEN inactivation; two patients carried pathogenic variants in the BRCA1 and BRCA2 genes.Conclusion. Genetic testing of young patients with breast fibroadenomas is important to optimize the management strategy in order to reduce cancer risk in high-risk groups of patients.
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来源期刊
Russian Journal of Pediatric Hematology and Oncology
Russian Journal of Pediatric Hematology and Oncology Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.40
自引率
0.00%
发文量
36
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