Hui Jessica, Zhan Xin, Bashir Amani, Policeni Fabiana, Kim Hsieh Su
Department of Radiology University of Iowa Hospitals and Clinics Iowa City Iowa USA.
Department of Pathology University of Iowa Hospitals and Clinics Iowa City Iowa USA.
Clin Case Rep. 2024 Aug 6;12(8):e9270. doi: 10.1002/ccr3.9270. eCollection 2024 Aug.
Epithelial-myoepithelial carcinoma of the breast is an extremely rare biphasic tumor. This report documents the first case of epithelial-myoepithelial carcinoma presenting in the location of a previously treated ductal carcinoma in order to increase the awareness of this entity as a potential differential for recurrent breast lesions.
Epithelial-myoepithelial carcinoma of the breast is an exceedingly rare biphasic tumor, seldom documented in medical literature. This report describes the first known case of this entity at the site of a previously treated neoplasm in a 75-year-old female with a history of high-grade ductal carcinoma in situ who presented with a new breast mass. Imaging demonstrated an oval shaped mass with microlobulated borders and hypoechoic echogenicity on ultrasound. Following multidisciplinary discussion, she underwent a mastectomy, revealing epithelial-myoepithelial carcinoma with metaplastic squamous cell carcinoma. The patient began chemotherapy but discontinued due to poor tolerance and neurological complications. Generally, prognosis for epithelial-myoepithelial carcinoma (World Health Organization Classification of Breast Tumors 2019, 8562/3) is highly variable, with limited available data suggesting that epithelial-myoepithelial carcinoma may follow a course similar to that of breast adenocarcinomas with both hematogenous and lymphatic spread. Treatment typically involves curative excision, though the role of axillary lymph node sampling remains under discussion. This case underscores the need for vigilance in post-treatment surveillance for breast cancer and highlights the importance of recognizing this entity in recurrent breast pathology.
乳腺上皮-肌上皮癌是一种极其罕见的双相性肿瘤。本报告记录了首例发生于既往治疗过的导管癌部位的上皮-肌上皮癌病例,以提高对该实体作为复发性乳腺病变潜在鉴别诊断的认识。
乳腺上皮-肌上皮癌是一种极为罕见的双相性肿瘤,在医学文献中鲜有记载。本报告描述了首例已知的该实体病例,发生于一名75岁女性既往治疗过的肿瘤部位,该女性有高级别原位导管癌病史,此次出现新的乳腺肿块。影像学检查显示超声下为椭圆形肿块,边界呈微分叶状,回声低。经过多学科讨论,她接受了乳房切除术,病理显示为上皮-肌上皮癌合并化生鳞状细胞癌。患者开始化疗,但因耐受性差和神经并发症而停药。一般来说,上皮-肌上皮癌(世界卫生组织2019年乳腺肿瘤分类,8562/3)的预后差异很大,有限的现有数据表明,上皮-肌上皮癌的病程可能与乳腺腺癌相似,有血行和淋巴转移。治疗通常包括根治性切除,不过腋窝淋巴结取样的作用仍在讨论中。本病例强调了乳腺癌治疗后监测需保持警惕的必要性,并突出了在复发性乳腺病理中识别该实体的重要性。