Zhou Peng, Zhang Qingqing, Zhu Jian, Li Peifeng
Department of Thyroid and Breast Surgery, The 960th Hospital of PLA, Jinan, 250031, China.
Department of Oncology, The 960th Hospital of PLA, Jinan, 250031, China.
Pathol Res Pract. 2021 Aug;224:153489. doi: 10.1016/j.prp.2021.153489. Epub 2021 May 24.
Phyllodes tumors of the breast are rare fibroepithelial tumors, and malignant phyllodes tumors occasionally exhibit heterogeneous differentiation. Here, we report a case of malignant phyllodes tumor with pleomorphic liposarcomatous differentiation, and examined the genomic features of both components using capture-based next-generation sequencing of 425 cancer-related genes. A 56-year-old woman presented with a palpable, asymptomatic nodule in the right breast measuring 4.0 cm × 3.0 cm. Based on the findings from microscopic examination, the lesions were identified as malignant phyllodes tumor and pleomorphic liposarcoma. The liposarcomatous differentiation component was positive for S-100, but had no MDM2 and CDK4 amplifications according to the results of fluorescence in situ hybridization. The malignant phyllodes tumor and liposarcomatous differentiation component had similar genetic mutations, such as TP53, TERT, EGFR, RARA, RB1, and MED12 mutations, all of which are common mutations in phyllodes tumors. These results indicate that the pathogenesis of the pleomorphic liposarcomatous differentiation was similar with that of phyllodes tumor, but was different from the pleomorphic liposarcoma in extramammary sites. Thus, the intratumoral heterogeneity may have independently evolved after tumorigenesis.
乳腺叶状肿瘤是罕见的纤维上皮性肿瘤,恶性叶状肿瘤偶尔表现出异质性分化。在此,我们报告一例具有多形性脂肪肉瘤样分化的恶性叶状肿瘤病例,并使用基于捕获的425个癌症相关基因的二代测序检测了两个成分的基因组特征。一名56岁女性右侧乳房出现一个可触及的无症状结节,大小为4.0 cm×3.0 cm。根据显微镜检查结果,病变被鉴定为恶性叶状肿瘤和多形性脂肪肉瘤。脂肪肉瘤样分化成分S-100呈阳性,但荧光原位杂交结果显示无MDM2和CDK4扩增。恶性叶状肿瘤和脂肪肉瘤样分化成分具有相似的基因突变,如TP53、TERT、EGFR、RARA、RB1和MED12突变,这些都是叶状肿瘤中的常见突变。这些结果表明,多形性脂肪肉瘤样分化的发病机制与叶状肿瘤相似,但与乳腺外部位的多形性脂肪肉瘤不同。因此,肿瘤内异质性可能在肿瘤发生后独立演变。