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1例乳腺叶状肿瘤合并脂肪肉瘤:病例报告及文献复习

A Case of Phyllodes Tumor of the Breast with Mixed Liposarcoma: Case Report and Literature Review.

作者信息

Tu He Ta Mi Shi Mei Er, Wang Ning, Yao Qing, Dong Shuang-Shuang, Feng Xiao, Zhao Jin, Zou Hong, Pang Li-Juan, Qi Yan

机构信息

Department of Pathology, Shihezi University School of Medicine and the First Affiliated Hospital to Shihezi University School of Medicine, Shihezi, Xinjiang, 832002, People's Republic of China.

Department of Pathology, Central People's Hospital of Zhanjiang and Zhanjiang Central Hospital, Guangdong Medical University, Zhanjiang, People's Republic of China.

出版信息

Onco Targets Ther. 2021 May 6;14:3003-3011. doi: 10.2147/OTT.S298379. eCollection 2021.

Abstract

Phyllodes tumors (PTs) account for less than 1% of breast tumors, and malignant PTs account for even less. Here, we described an unusual case of malignant PT with mixed liposarcoma (myxoid liposarcoma [MLP] and pleomorphic liposarcoma [PLP]). A 52-year-old woman discovered a small lump in her left breast. Twenty years later, the lump suddenly grew within 1 month. Mammography showed space-occupying lesions of the left breast. Histologically, the tumor was characterized by hypercellular stroma covering the epithelium and protrusion of the myoepithelium into the cyst to form a lobulated structure; regions of loose mucus and hypercellular structures alternated. A region of peripheral benign fibroadenoma was also observed, and many stellate and spindle cells or signet ring-like cells were identified in loose areas. Some areas showed a characteristic thin branching vascular pattern. In the cell-rich area, adipocytes and odd megakaryocytes were observed. Atypical mitotic figures were observed in the cell-rich and mucus areas (16 mitoses/10 high-power fields [HPF] and 2 mitoses/10 HPF, respectively). In the immunohistochemical analysis, a small number of tumor cells were positive for AE1/3 and vimentin, whereas all cells were negative for cytokeratin 34βE12, E-cadherin, p63, estrogen receptor, progesterone receptor, human epidermal growth factor receptor 2, and S-100, ruling out the possibility of metaplastic carcinoma. Interestingly, cyclin-dependent kinase 4, mouse double minute 2 (MDM2), and p16 were strongly positive in both loose mucus and cell-rich areas. However, the fluorescence in situ hybridization test results showed that MDM2 was not amplified. Combined with morphological characteristics, these findings supported that the tumor was a mixed malignant PT with MLP and PLP. Our patient did not receive radiation therapy, and after 47 months of follow-up, no recurrence or metastasis occurred. This case report serves to expand the morphologic spectrum of mixed malignant PT with liposarcoma.

摘要

叶状肿瘤(PTs)占乳腺肿瘤的比例不到1%,而恶性PTs所占比例更低。在此,我们描述了一例罕见的伴有混合性脂肪肉瘤(黏液样脂肪肉瘤[MLP]和多形性脂肪肉瘤[PLP])的恶性PT病例。一名52岁女性在其左乳发现一个小肿块。20年后,该肿块在1个月内突然增大。乳腺钼靶检查显示左乳占位性病变。组织学上,肿瘤的特征为覆盖上皮的细胞丰富的间质以及肌上皮向囊肿内突出形成分叶状结构;疏松黏液区域和细胞丰富区域交替出现。还观察到周边有良性纤维腺瘤区域,在疏松区域发现许多星状和梭形细胞或印戒样细胞。一些区域呈现出特征性的细分支血管模式。在细胞丰富区域,观察到脂肪细胞和怪异的巨核细胞。在细胞丰富区域和黏液区域观察到非典型有丝分裂象(分别为16个有丝分裂象/10个高倍视野[HPF]和2个有丝分裂象/10个HPF)。免疫组化分析显示,少数肿瘤细胞AE1/3和波形蛋白呈阳性,而所有细胞细胞角蛋白34βE12、E-钙黏蛋白、p63、雌激素受体、孕激素受体、人表皮生长因子受体2和S-100均为阴性,排除了化生性癌的可能性。有趣的是,细胞周期蛋白依赖性激酶4、小鼠双微体2(MDM2)和p16在疏松黏液区域和细胞丰富区域均呈强阳性。然而,荧光原位杂交检测结果显示MDM2未扩增。结合形态学特征,这些发现支持该肿瘤为伴有MLP和PLP的混合性恶性PT。我们的患者未接受放射治疗,经过47个月的随访,未出现复发或转移。本病例报告有助于扩展伴有脂肪肉瘤的混合性恶性PT的形态学谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b1/8110257/ec37c86dbc95/OTT-14-3003-g0001.jpg

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