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首页> 外文期刊>American Journal of Case Reports >Rare Human Epidermal Growth Factor Receptor 2 (HER-2)-Positive Neuroendocrine Carcinoma of the Breast: A Case Report with 9-Year Follow-up
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Rare Human Epidermal Growth Factor Receptor 2 (HER-2)-Positive Neuroendocrine Carcinoma of the Breast: A Case Report with 9-Year Follow-up

机译:稀有人体表皮生长因子受体2(HER-2) - 乳腺的阳性神经内分泌癌:一个案例报告,9年后续随访

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Patient: Female, 70-year-old Final Diagnosis: Neuroendocrine carcinoma of the breast Symptoms: None Medication:— Clinical Procedure: — Specialty: Oncology Objective: Rare disease Background: Neuroendocrine carcinoma of the breast (NECB) is very rare, accounting for 0.1% of all breast tumors and less than 1% of all neuroendocrine tumors. Most NECBs are hormone receptor-positive and human epidermal growth factor receptor 2 (HER-2)-negative and more than 50% are the luminal B subtype. Because prospective studies of NECB are lacking, treatment is the same as for other breast tumors. Case Report: A 70-year-old woman was diagnosed with NECB in February 2011. She underwent radical right mastectomy and right axillary node dissection. Final histopathological examination revealed NECB with positive axillary nodes (N1). The tumor cells were 100% positive for estrogen receptors and 10% positive for progesterone receptors. The HER-2 status was 3+. According to the Tumor, Node, Metastasis (TNM) Classification of Malignant Tumors, the pathologic stage was IIB - pT2pN1cM0. The histologic grade was 2 and the Ki-67 proliferation index was 5.7%. The patient received adjuvant chemotherapy, radiation therapy, IV trastuzumab, and endocrine therapy. After 9 years of follow-up, she remains disease-free. Conclusions: As far as we know, this is only the second report describing treatment of HER-2-positive NECB with trastuzumab. A literature review shows that it is the first report of treatment of HER-2-positive primary NECB with adjuvant trastuzumab. In similar cases, long-term follow-up is recommended because of the potential for multiple metastases of NECB even years after completion of adjuvant therapy.
机译:患者:女性,70岁的最终诊断:神经内分泌癌的乳腺症状:无药物: - 临床手术: - 专业:肿瘤学目标:稀有疾病背景:乳房(NECB)神经内分泌癌是非常罕见的,核算所有乳腺肿瘤的0.1%,占所有神经内分泌肿瘤的1%。大多数NECB是激素受体阳性和人表皮生长因子受体2(HER-2) - 高于50%的是腔B亚型。由于缺乏对NECB的前瞻性研究,治疗与其他乳腺肿瘤相同。案例报告:2011年2月,一名70岁的女性被诊断为NECB。她接受了激进的乳房切除术和右腋窝节点解剖。最终组织病理学检查显示NECB具有阳性腋窝节点(N1)。肿瘤细胞为雌激素受体100%阳性,孕酮受体10%阳性。 HER-2状态为3+。根据肿瘤,节点,转移(TNM)分类恶性肿瘤,病理阶段是IIB - PT2PN1CM0。组织学等分为2,Ki-67增殖指数为5.7%。患者接受了辅助化疗,放射治疗,IV曲妥珠单抗和内分泌治疗。经过9年的后续后,她仍然没有疾病。结论:据我们所知,这只是描述了用曲妥珠单抗治疗Her-2阳性NECB的第二次报告。文献综述表明,它是用佐剂曲妥珠单抗治疗Her-2阳性原发性NECB的第一报告。在类似的情况下,推荐长期随访,因为辅助治疗完成后Necb甚至多年的多重转移。

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