Primary neuroendocrine tumors of the breast: two case reports and review of the literature

Abstract Background 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 present...

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Main Authors: Loubna Hejjane, Karima Oualla, Zineb Bouchbika, Mouna Bourhafour, Anas Lhlou Mimi, Efared Boubacar, Abdellatif Benider, Zineb Benbrahim, Samia Aarifi, Nawef Mellas
Format: Article
Language:English
Published: BMC 2020-03-01
Series:Journal of Medical Case Reports
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13256-020-02361-5
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author Loubna Hejjane
Karima Oualla
Zineb Bouchbika
Mouna Bourhafour
Anas Lhlou Mimi
Efared Boubacar
Abdellatif Benider
Zineb Benbrahim
Samia Aarifi
Nawef Mellas
author_facet Loubna Hejjane
Karima Oualla
Zineb Bouchbika
Mouna Bourhafour
Anas Lhlou Mimi
Efared Boubacar
Abdellatif Benider
Zineb Benbrahim
Samia Aarifi
Nawef Mellas
author_sort Loubna Hejjane
collection DOAJ
description Abstract Background 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 presentation 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. Conclusion 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.
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spelling doaj.art-034371f9d9b54d98a3926584936cfba32022-12-22T03:40:29ZengBMCJournal of Medical Case Reports1752-19472020-03-011411610.1186/s13256-020-02361-5Primary neuroendocrine tumors of the breast: two case reports and review of the literatureLoubna Hejjane0Karima Oualla1Zineb Bouchbika2Mouna Bourhafour3Anas Lhlou Mimi4Efared Boubacar5Abdellatif Benider6Zineb Benbrahim7Samia Aarifi8Nawef Mellas9Mohammed VI Center for Cancer Treatment, Ibn Rochd University HospitalDepartment of Oncology Medical, Hassan II University HospitalMohammed VI Center for Cancer Treatment, Ibn Rochd University HospitalMohammed VI Center for Cancer Treatment, Ibn Rochd University HospitalDepartment of Radiology, Hassan II University HospitalDepartment of Pathology, Hassan II University HospitalMohammed VI Center for Cancer Treatment, Ibn Rochd University HospitalDepartment of Oncology Medical, Hassan II University HospitalDepartment of Oncology Medical, Hassan II University HospitalDepartment of Oncology Medical, Hassan II University HospitalAbstract Background 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 presentation 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. Conclusion 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.http://link.springer.com/article/10.1186/s13256-020-02361-5Neuroendocrine carcinomaBreast cancerCase reportChromograninImmunohistochemistry
spellingShingle Loubna Hejjane
Karima Oualla
Zineb Bouchbika
Mouna Bourhafour
Anas Lhlou Mimi
Efared Boubacar
Abdellatif Benider
Zineb Benbrahim
Samia Aarifi
Nawef Mellas
Primary neuroendocrine tumors of the breast: two case reports and review of the literature
Journal of Medical Case Reports
Neuroendocrine carcinoma
Breast cancer
Case report
Chromogranin
Immunohistochemistry
title Primary neuroendocrine tumors of the breast: two case reports and review of the literature
title_full Primary neuroendocrine tumors of the breast: two case reports and review of the literature
title_fullStr Primary neuroendocrine tumors of the breast: two case reports and review of the literature
title_full_unstemmed Primary neuroendocrine tumors of the breast: two case reports and review of the literature
title_short Primary neuroendocrine tumors of the breast: two case reports and review of the literature
title_sort primary neuroendocrine tumors of the breast two case reports and review of the literature
topic Neuroendocrine carcinoma
Breast cancer
Case report
Chromogranin
Immunohistochemistry
url http://link.springer.com/article/10.1186/s13256-020-02361-5
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