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病例报告:乳腺神经内分泌癌——文献综述及6例病例展示

Case Report: Neuroendocrine carcinoma of the breast: a review of the literature and illustration of six cases.

作者信息

Albayrak Nazire E

机构信息

Department of Pathology, Molecular and Cell-Based Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

出版信息

Front Med (Lausanne). 2025 Aug 20;12:1551309. doi: 10.3389/fmed.2025.1551309. eCollection 2025.

Abstract

"Primary neuroendocrine breast carcinoma (NEBC) is an underdiagnosed subtype of breast cancer, which includes small cell (SCNEC) and large cell neuroendocrine carcinomas (LCNEC). Accurate diagnosis remains challenging given their low incidence; misclassification as invasive breast carcinoma of no special type (IBC-NST), invasive ductal carcinoma (IDC), or a metastatic neuroendocrine carcinoma may occur. Cases with any component of adenocarcinoma and well-differentiated neuroendocrine tumors were excluded. A search of the pathology database (2012-2024) revealed six female patients (27-85 years) with a final pathologic diagnosis of NEBC (stages IA-IV), including four diagnosed with LCNEC and two with SCNEC. Even though most NEBC cases (5 of 6; 83%) were of the luminal subtype, five of six patients (83%) developed distant metastases within 4 years of the initial diagnosis. Molecular profiling of six cases revealed common alterations in the FGF/FGFR and PI3K/AKT/mTOR pathways. In summary, primary neuroendocrine carcinomas of the breast display aggressive behavior. However, they are more likely to harbor certain alterations, such as activating mutations and amplification, which can be of therapeutic value. The Ki-67 index, unlike in the pancreas and gastrointestinal tract, is not suitable for grading neuroendocrine neoplasms (NENs) of the breast. However, it can still serve as a tool for risk stratification, similar to its use in luminal-type breast cancer.

摘要

原发性神经内分泌乳腺癌(NEBC)是一种诊断不足的乳腺癌亚型,包括小细胞神经内分泌癌(SCNEC)和大细胞神经内分泌癌(LCNEC)。鉴于其发病率低,准确诊断仍然具有挑战性;可能会被误诊为非特殊类型浸润性乳腺癌(IBC-NST)、浸润性导管癌(IDC)或转移性神经内分泌癌。排除了含有腺癌和高分化神经内分泌肿瘤任何成分的病例。检索病理数据库(2012 - 2024年)发现6例女性患者(27 - 85岁),最终病理诊断为NEBC(IA - IV期),其中4例诊断为LCNEC,2例诊断为SCNEC。尽管大多数NEBC病例(6例中的5例;83%)为管腔亚型,但6例患者中有5例(83%)在初始诊断后4年内发生远处转移。6例病例的分子谱分析显示FGF/FGFR和PI3K/AKT/mTOR通路存在常见改变。总之,原发性乳腺神经内分泌癌表现出侵袭性。然而,它们更有可能存在某些改变,如激活突变和扩增,这可能具有治疗价值。与胰腺和胃肠道不同,Ki-67指数不适用于乳腺神经内分泌肿瘤(NENs)的分级。然而,它仍然可以作为风险分层的工具,类似于其在管腔型乳腺癌中的应用。

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