Bai Caiyun, Xin Xiaodong, Yang Yisen, Qu Fengjiang, Fan Zhimin
Breast Surgery Department, General Surgery Center, The First Hospital of Jilin University, Changchun, China.
Emergency Surgery Department, The First Hospital of Jilin University, Changchun, China.
Front Oncol. 2025 Feb 20;14:1497272. doi: 10.3389/fonc.2024.1497272. eCollection 2024.
Acinic cell carcinoma (AcCC) of the breast is an extremely rare malignant epithelial tumor characterized by acini cell differentiation, clinical low-grade malignancy, and a molecular triple-negative subtype.
A 47-year-old female presented with a 1-month history of a painless mass in her right breast.
Ultrasound imaging, mammography and magnetic resonance imaging revealed a lesion, approximately 3.0cm×1.5cm in size, in the right breast, which was considered to be a malignancy. After the surgery, the AcCC of the breast was confirmed histologically.
Right breast mastectomy and sentinel lymph node biopsy were performed. Adjuvant chemotherapy included 4 cycles of doxorubicin hydrochloride (Adriamycin) and cyclophosphamide followed by 4 cycles of docetaxel (Taxotere).
The patient was discharged from the hospital after surgery. There was no sign of recurrence during a 9-month follow-up period.
Acinic cell carcinoma (AcCC) of the breast is an extremely rare malignant epithelial tumor that can be accurately diagnosed based on histopathologic morphology and immunohistochemistry. The weak positive progesterone receptor (PR) expressed in this case is extremely rare, which may provide a new research direction for the endocrine therapy of AcCC. Both AcCC and microglandular adenosis(MGA) exhibit microglandular growth, and the relationship between them remains unclear. Differentiation between them not only relies on histomorphology and pathological immunohistochemistry but also depends on clinical manifestations and other presentations. Optimal treatment of AcCC is the same as that for invasive breast cancer. The prognosis is generally good, with adjuvant therapy after surgery.
乳腺腺泡细胞癌(AcCC)是一种极其罕见的恶性上皮性肿瘤,其特征为腺泡细胞分化、临床低度恶性以及分子三阴性亚型。
一名47岁女性,右乳出现无痛性肿块1个月。
超声成像、乳腺钼靶和磁共振成像显示右乳有一大小约3.0cm×1.5cm的病变,考虑为恶性。术后经组织学证实为乳腺AcCC。
行右乳乳房切除术及前哨淋巴结活检。辅助化疗包括4个周期的盐酸多柔比星(阿霉素)和环磷酰胺,随后是4个周期的多西他赛(泰索帝)。
患者术后出院。在9个月的随访期内无复发迹象。
乳腺腺泡细胞癌(AcCC)是一种极其罕见的恶性上皮性肿瘤,可根据组织病理形态和免疫组化准确诊断。本例中孕激素受体(PR)呈弱阳性极为罕见,这可能为AcCC的内分泌治疗提供新的研究方向。AcCC和微腺性腺病(MGA)均表现为微腺性生长,它们之间的关系尚不清楚。两者的鉴别不仅依赖于组织形态学和病理免疫组化,还取决于临床表现等。AcCC的最佳治疗与浸润性乳腺癌相同。术后进行辅助治疗,预后一般良好。