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Primary pleomorphic rhabdomyosarcoma of breast: Report of a rare neoplasm

机译:乳腺原发性多形性横纹肌肉瘤:罕见肿瘤报告

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摘要

Primary sarcoma of the breast is very rare and constitutes less than 1% of all breast cancers. Herein, we report a case of pleomorphic rhabdomyosarcoma (PRMS) of the right breast in a 49-year-old female patient presented with a mass (7 cm x 6.5 cm). Mammography and ultrasonography suspected a malignant lesion and a diagnosis of poorly differentiated carcinoma was made on fine needle aspiration cytology. Modified radical mastectomy was carried out. Histopathological examination revealed a high grade stromal sarcoma with rhabdoid morphology and multinucleated tumor giant cells. The tumor cells were strongly positive for desmin, vimentin and Myo D1 focally. The tumor cells were immunonegative for cytokeratin, epithelial membrane antigen (EMA), CD34, CD45, SMA, S100, CD68 and HMB45. A final diagnosis of PRMS was rendered. Surgical margins were free and no metastasis was seen in axillary lymph nodes. Neither post-operative radiotherapy nor adjuvant chemotherapy was given and the patient has remained disease free 12 months post-operatively.
机译:乳腺癌的原发性肉瘤非常罕见,占所有乳腺癌的不到1%。本文中,我们报告了一名49岁女性患者,其肿块(7厘米x 6.5厘米)出现右乳状多形性横纹肌肉瘤(PRMS)。钼靶和超声检查怀疑为恶性病变,并根据细针穿刺细胞学检查诊断为低分化癌。进行了改良的根治性乳房切除术。组织病理学检查显示具有横纹肌样形态和多核肿瘤巨细胞的高度间质肉瘤。肿瘤细胞对结蛋白,波形蛋白和Myo D1呈强阳性。肿瘤细胞对细胞角蛋白,上皮膜抗原(EMA),CD34,CD45,SMA,S100,CD68和HMB45呈免疫阴性。对PRMS做出了最终诊断。手术切缘无,腋窝淋巴结未见转移。既未进行术后放疗,也未进行辅助化疗,并且患者在术后12个月仍无疾病。

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