Hejjane Loubna, Oualla Karima, Bouchbika Zineb, Bourhafour Mouna, Lhlou Mimi Anas, Boubacar Efared, Benider Abdellatif, Benbrahim Zineb, Aarifi Samia, Mellas Nawef
Mohammed VI Center for Cancer Treatment, Ibn Rochd University Hospital, Casablanca, Morocco.
Department of Oncology Medical, Hassan II University Hospital, Fez, Morocco.
J Med Case Rep. 2020 Mar 10;14(1):41. doi: 10.1186/s13256-020-02361-5.
Neuroendocrine carcinomas mainly affect the bronchopulmonary and the gastrointestinal systems. Breast localizations are very rare. They represent less than 0.1% of all breast cancers. A definitive diagnosis relies on histological and immunohistochemical examinations.
Case 1 We report a case of primary neuroendocrine carcinoma of the breast in a 71-year-old Arabic woman who presented with a 3 cm palpable and mobile tumor of the right breast. Clinical and radiological assessment excluded any other primary tumor. Radical mastectomy and axillary lymph node resection were performed. A histopathological examination disclosed the diagnosis of primary breast neuroendocrine tumors, with negative surgical margins and lymph nodes (18 N-/18 N). The tumor cells were positive for neuroendocrine markers, a weak Ki-67 proliferation index and negative Her2/neu. Our patient received adjuvant hormonal treatment with anti-aromatase for 21 months. She is on regular follow-up, and she remains free of disease to date. Case 2 A 48-year-old Arabic woman consulted for a right breast nodule. She underwent lumpectomy with right axillary lymphadenectomy. The diagnosis was breast neuroendocrine tumor. Systemic treatment was proposed, but she was lost to follow-up. She consulted 1 year later for a mass in the same breast. A histological and immunohistochemical examination of a mammary biopsy was consistent with a recurrence of the previous neuroendocrine tumor. A radiological assessment showed a large mass in her right breast, ipsilateral axillary lymphadenopathies, and hepatic and pulmonary metastases. She received first-line metastatic chemotherapy, with good clinical and radiological improvement. She refused the mastectomy and was given hormone therapy. One year later, the tumor expanded clinically and radiologically, and she underwent second-line metastatic chemotherapy, with good clinical progress and radiological stability, and she then underwent maintenance hormonal therapy.
Due to the rarity of primary breast neuroendocrine tumors, no standard therapy exists and the prognosis remains difficult to determine. Studies, including larger series, are needed in order to understand the biological behavior of these tumors.
神经内分泌癌主要累及支气管肺和胃肠系统。乳腺部位的神经内分泌癌非常罕见,占所有乳腺癌的比例不到0.1%。明确诊断依赖于组织学和免疫组化检查。
病例1 我们报告一例71岁阿拉伯女性原发性乳腺神经内分泌癌,患者右乳可触及一个3厘米可活动的肿块。临床和影像学评估排除了任何其他原发性肿瘤。行根治性乳房切除术和腋窝淋巴结切除术。组织病理学检查确诊为原发性乳腺神经内分泌肿瘤,手术切缘和淋巴结均为阴性(18枚淋巴结阴性/18枚淋巴结)。肿瘤细胞神经内分泌标志物呈阳性,Ki-67增殖指数低,Her2/neu呈阴性。我们的患者接受了21个月的芳香化酶抑制剂辅助内分泌治疗。她定期接受随访,至今仍无疾病复发。病例2 一名48岁阿拉伯女性因右乳结节就诊。她接受了肿块切除术及右腋窝淋巴结清扫术。诊断为乳腺神经内分泌肿瘤。建议进行全身治疗,但她失访了。1年后,她因同一乳房出现肿块再次就诊。乳腺活检的组织学和免疫组化检查结果与之前的神经内分泌肿瘤复发一致。影像学评估显示右乳有一个大肿块,同侧腋窝淋巴结肿大,并有肝和肺转移。她接受了一线转移性化疗,临床和影像学均有良好改善。她拒绝了乳房切除术,接受了激素治疗。1年后,肿瘤在临床和影像学上均有进展,她接受了二线转移性化疗,临床进展良好,影像学稳定,随后接受了维持性激素治疗。
由于原发性乳腺神经内分泌肿瘤罕见,目前尚无标准治疗方案,预后仍难以确定。需要开展包括更大样本量的研究,以了解这些肿瘤的生物学行为。