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伴有甲胎蛋白显著升高的原发性乳腺神经内分泌癌:一例报告

Primary neuroendocrine carcinoma of the breast with markedly elevated alpha-fetoprotein: a case report.

作者信息

Wang Jia, Wang Xichen, Du Wenlong, Guo Yuanxian, Yang Xiaoping, Pan Jiebin, Yin Lanning

机构信息

Department of General Surgery, Lanzhou University Second Hospital, Lanzhou, China.

Department of General Surgery, Xigu District of Lanzhou City People's Hospital, Lanzhou, China.

出版信息

Transl Cancer Res. 2021 May;10(5):2503-2508. doi: 10.21037/tcr-20-3391.

Abstract

Primary neuroendocrine carcinoma of the breast (PNECB) is a relatively rare subtype of breast cancer that has seldom been studied since its initial description. At present, the pathogenesis of the disease remains unknown, and there exit no specific clinical guidelines or specifications for its diagnosis and treatment. In addition, alpha-fetoprotein (AFP)-despite being a tumor marker-plays a small role in the diagnosis of breast cancer. Here, we explain the diagnosis and treatment of primary neuroendocrine (NE) breast carcinoma in a patient with a markedly elevated level of AFP. A 52-year-old woman visited our hospital, reporting she had palpated a nodule in her left breast 1 day before admission. After ultrasonographic detection of the hypoechoic lesion in her left breast-which was classified according to the Breast Imaging Reporting and Data System (BI-RADS) as grade 4C-and the abnormal enlargement of her left axillary lymph nodes, the patient was referred to our department as a case of malignant breast tumor. Meanwhile, the level of the tumor marker AFP was found to be over 1,210 ng/mL (0-7 ng/mL). And the patient had no past medical history of increased AFP, abnormal liver function, or gastrointestinal tumor. Analysis of the surgical specimens obtained from the left breast showed grade II invasive ductal carcinoma with NE differentiation. After discussion with a multidisciplinary team (MDT), according to the results of pathological and immunohistochemical examinations, the patient was diagnosed with PNECB. Due to axillary lymph node metastasis, she received combined chemotherapy with cyclophosphamide, epirubicin, and paclitaxel on postoperative day 13. Up to now, six cycles of chemotherapy have been successfully administered, with no evidence of adverse reactions. AFP levels were all above 1,210 ng/mL during chemotherapy. At the time of submission, the patient has been followed up for 10 months and there has been axillary lymph node metastasis, but no tumors in other parts have been found. Therefore, we think that the increase in AFP levels is related to the occurrence and poor prognosis of PNECB.

摘要

原发性乳腺神经内分泌癌(PNECB)是乳腺癌中一种相对罕见的亚型,自首次被描述以来很少被研究。目前,该疾病的发病机制尚不清楚,并且对于其诊断和治疗没有特定的临床指南或规范。此外,甲胎蛋白(AFP)——尽管是一种肿瘤标志物——在乳腺癌诊断中作用不大。在此,我们阐述了一名AFP水平显著升高的原发性神经内分泌(NE)乳腺癌患者的诊断和治疗情况。一名52岁女性入院前1天前来我院就诊,称其左侧乳房摸到一个结节。在超声检测到左侧乳房低回声病变(根据乳腺影像报告和数据系统(BI-RADS)分类为4C级)以及左侧腋窝淋巴结异常肿大后,该患者作为乳腺恶性肿瘤病例被转诊至我科。同时,发现肿瘤标志物AFP水平超过1210 ng/mL(0 - 7 ng/mL)。且该患者既往无AFP升高、肝功能异常或胃肠道肿瘤病史。对左侧乳房手术标本的分析显示为伴有NE分化的II级浸润性导管癌。经多学科团队(MDT)讨论,根据病理和免疫组化检查结果,该患者被诊断为PNECB。由于腋窝淋巴结转移,她在术后第13天接受了环磷酰胺、表柔比星和紫杉醇联合化疗。截至目前,已成功进行了六个周期的化疗,无不良反应迹象。化疗期间AFP水平均高于1210 ng/mL。在提交本文时,该患者已随访10个月,存在腋窝淋巴结转移,但未发现其他部位有肿瘤。因此,我们认为AFP水平升高与PNECB的发生及预后不良有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e847/8798033/754f238616e9/tcr-10-05-2503-f1.jpg

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