Primary small cell neuroendocrine carcinoma of the breast : a report of two cases and review of literature

Spinelli C, Fregoli L, Biricotti M, Pucci V, Grosso M, O. F, Spisni R, Usolini C, Caldarelli C
{"title":"Primary small cell neuroendocrine carcinoma of the breast : a report of two cases and review of literature","authors":"Spinelli C, Fregoli L, Biricotti M, Pucci V, Grosso M, O. F, Spisni R, Usolini C, Caldarelli C","doi":"10.14312/2052-4994.2013-28","DOIUrl":null,"url":null,"abstract":"Primary neuroendocrine carcinomas of the breast are extremely rare. Neuroendocrine tumors mainly occur in the broncopolmonary system and gastrointestinal tract. The diagnosis of small cell neuroendocrine carcinoma (SCNC) of the breast can only be made if a non mammary site is excluded or if an in situ component can be found. We are going to describe two cases and to discuss their clinical, radiological and pathological manifestations. Introduction: Neuroendocrine tumors are rare and slow-growing neoplasias derived from neuroendocrine cells. We describe two cases of small cell neuroendocrine carcinoma of the breast and discuss their clinical, radiological and pathological manifestations. Case report: Our patients are two Italian females (38 and 36 year-old) with no family history of breast disease. In both cases the diagnosis was confirmed after surgery, when immunohistochemistry revealed a neuroendocrine differentiation of the tumor. The patients are alive and disease free after more than ten years of follow-up. Conclusion: Primary neuroendocrine carcinomas of the breast are extremely rare. The diagnosis of SCNC of the breast can only be made if a non mammary site is excluded or if an in situ component can be found. After surgery, a strict follow-up including octreotide scan should be performed and this doesn’t differ from the one of the usual breast carcinoma.","PeriodicalId":90205,"journal":{"name":"Journal of cancer research & therapy","volume":"115 1","pages":"186-193"},"PeriodicalIF":0.0000,"publicationDate":"2013-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of cancer research & therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14312/2052-4994.2013-28","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Primary neuroendocrine carcinomas of the breast are extremely rare. Neuroendocrine tumors mainly occur in the broncopolmonary system and gastrointestinal tract. The diagnosis of small cell neuroendocrine carcinoma (SCNC) of the breast can only be made if a non mammary site is excluded or if an in situ component can be found. We are going to describe two cases and to discuss their clinical, radiological and pathological manifestations. Introduction: Neuroendocrine tumors are rare and slow-growing neoplasias derived from neuroendocrine cells. We describe two cases of small cell neuroendocrine carcinoma of the breast and discuss their clinical, radiological and pathological manifestations. Case report: Our patients are two Italian females (38 and 36 year-old) with no family history of breast disease. In both cases the diagnosis was confirmed after surgery, when immunohistochemistry revealed a neuroendocrine differentiation of the tumor. The patients are alive and disease free after more than ten years of follow-up. Conclusion: Primary neuroendocrine carcinomas of the breast are extremely rare. The diagnosis of SCNC of the breast can only be made if a non mammary site is excluded or if an in situ component can be found. After surgery, a strict follow-up including octreotide scan should be performed and this doesn’t differ from the one of the usual breast carcinoma.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
乳腺原发性小细胞神经内分泌癌2例报告并文献复习
原发性乳腺神经内分泌癌极为罕见。神经内分泌肿瘤主要发生在支气管肺系统和胃肠道。乳腺小细胞神经内分泌癌(SCNC)的诊断只能在排除非乳腺部位或发现原位成分的情况下进行。我们将描述两个病例,并讨论他们的临床,放射学和病理表现。神经内分泌肿瘤是一种罕见的生长缓慢的肿瘤,起源于神经内分泌细胞。我们报告两例乳腺小细胞神经内分泌癌,并讨论其临床、影像学及病理表现。病例报告:我们的患者是两名意大利女性(38岁和36岁),无乳腺家族史。在这两个病例的诊断是在手术后,当免疫组织化学显示肿瘤的神经内分泌分化。经过十多年的随访,患者存活且无疾病。结论:原发性乳腺神经内分泌癌极为罕见。乳腺SCNC的诊断只能在排除非乳腺部位或发现原位成分的情况下进行。手术后,应进行严格的随访,包括奥曲肽扫描,这与通常的乳腺癌没有什么不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Vulva and lower limb cancer: Results of inguinal lymph node staging on 81 cases Advances in artificial neural networks as a disease prediction tool Deuterium depletion inhibits lung cancer cell growth and migration in vitro and results in severalfold increase of median survival time of non-small cell lung cancer patients receiving conventional therapy Unique challenges and the changing face of oncology during the COVID-19 pandemic and beyond Variability in the metabolism of saccharides in bladder and colon cancer cell lines
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1