一例年轻乳腺间时癌和肉瘤诊断为李-弗劳梅尼综合征

Oncogen Pub Date : 2019-01-15 DOI:10.35702/ONC.10004
Seidler Sj, H. De
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摘要

与老年患者相比,遗传性和家族性癌症综合征在年轻患者中更为普遍。BRCA1和BRCA2突变约占年轻女性所有癌症病例的10%。尽管如此,早期发病的癌症可能是Li-Fraumeni综合征(LFS)的最初表现。LFS也被称为肉瘤、乳腺癌、白血病和肾上腺(SBLA)癌症综合征,由TP53基因的种系突变引起,导致广泛的早发性恶性肿瘤[3]。其传播为常染色体显性遗传,在普通人群中的患病率约为1/100000,占所有乳腺癌的1%。一半的受影响女性将在30岁时患上癌症,种系TP53突变的外显率达到100%。癌症是LFS患者中最常见的成人恶性肿瘤[4]。
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Breast Metachronous Carcinoma and Sarcoma in a Young Patient Leading to the Diagnosis of Li-Fraumeni Syndrome
Genetic and familial cancer syndromes are more prevalent in young patients compared to older counterparts. BRCA1 and BRCA2 mutations account for about 10% of all breast cancer cases in young women. Nevertheless, very early onset breast cancer might be the initial presentation of Li-Fraumeni syndrome (LFS). LFS is also known as sarcoma, breast, leukemia and adrenal gland (SBLA) cancer syndrome and is caused by the germline mutation of the TP53 gene, responsible for a wide spectrum of early-onset malignancies [3]. Its transmission is autosomal dominant with a prevalence of around 1/100000 in the general population and 1% of all breast cancers. Half of affected women will develop a cancer by the age 30 and the penetrance of the germline TP53 mutation reaches 100%. Breast cancer is the most common adult malignancy among patients with LFS [4].
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