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

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: C...

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Autores principales: Hejjane, Loubna, Oualla, Karima, Bouchbika, Zineb, Bourhafour, Mouna, Lhlou Mimi, Anas, Boubacar, Efared, Benider, Abdellatif, Benbrahim, Zineb, Aarifi, Samia, Mellas, Nawef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065345/
https://www.ncbi.nlm.nih.gov/pubmed/32156307
http://dx.doi.org/10.1186/s13256-020-02361-5
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author Hejjane, Loubna
Oualla, Karima
Bouchbika, Zineb
Bourhafour, Mouna
Lhlou Mimi, Anas
Boubacar, Efared
Benider, Abdellatif
Benbrahim, Zineb
Aarifi, Samia
Mellas, Nawef
author_facet Hejjane, Loubna
Oualla, Karima
Bouchbika, Zineb
Bourhafour, Mouna
Lhlou Mimi, Anas
Boubacar, Efared
Benider, Abdellatif
Benbrahim, Zineb
Aarifi, Samia
Mellas, Nawef
author_sort Hejjane, Loubna
collection PubMed
description 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 pubmed-70653452020-03-16 Primary neuroendocrine tumors of the breast: two case reports and review of the literature Hejjane, Loubna Oualla, Karima Bouchbika, Zineb Bourhafour, Mouna Lhlou Mimi, Anas Boubacar, Efared Benider, Abdellatif Benbrahim, Zineb Aarifi, Samia Mellas, Nawef J Med Case Rep Case Report 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. BioMed Central 2020-03-10 /pmc/articles/PMC7065345/ /pubmed/32156307 http://dx.doi.org/10.1186/s13256-020-02361-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Hejjane, Loubna
Oualla, Karima
Bouchbika, Zineb
Bourhafour, Mouna
Lhlou Mimi, Anas
Boubacar, Efared
Benider, Abdellatif
Benbrahim, Zineb
Aarifi, Samia
Mellas, Nawef
Primary neuroendocrine tumors of the breast: two case reports and review of the literature
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 Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065345/
https://www.ncbi.nlm.nih.gov/pubmed/32156307
http://dx.doi.org/10.1186/s13256-020-02361-5
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