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同步性乳腺实性神经内分泌癌和腹部淋巴瘤:一例报告并文献复习

Synchronous solid neuroendocrine breast carcinoma and abdominal lymphoma: A case report and review of the literature.

作者信息

Alonso-Ruano Miguel, López-Bonet Eugeni, Huerta-Anaya Maria Victoria, Vila-Camps Ester, Bernadó Luis, Tuca-Rodríguez Francesc, Suarez-Pumariega Pedro, Menendez Javier A

机构信息

Departments of Gynecology, Dr Josep Trueta Hospital of Girona, Girona; Catalonia, Spain.

出版信息

Oncol Lett. 2013 Feb;5(2):459-462. doi: 10.3892/ol.2012.1044. Epub 2012 Nov 23.

Abstract

Neuroendocrine tumors (NETs) are frequently associated with second primary malignancies (SPMs). Earlier studies have demonstrated that NETs are highly associated with synchronous or metachronous gastrointestinal and genitourinary SPMs. We report, for the first time, a case of pure NE breast carcinoma (NEBC) exhibiting all of the World Health Organization (WHO)-categorized morphological and phenotypic NE features (i.e., round solid nests of spindle cells, plasmacytoid cells, large clear or mucinous signet-ring cells with a peripheral palisading tendency and immunohistochemical positivity for the NE markers synaptophysin and chromogranin in more than 50% of the tumor cell population) along with synchronous abdominal non-Hodgkin's lymphoma. In the present study, we review the diagnosis, clinicopathological features and histogenetic profiling of NEBC and discuss the literature relevant to the clinical and anatomopathological management of this case. This previously unreported case of synchronous solid NEBC and abdominal lymphoma, together with earlier studies showing that primary symptoms are caused by SPMs in a significant subgroup of NET patients, strongly supports the notion that NETs should be cautiously considered to be index tumors. Therefore, risk-adapted clinicopathological follow-up with systematic investigation is strongly recommended.

摘要

神经内分泌肿瘤(NETs)常与第二原发性恶性肿瘤(SPMs)相关。早期研究表明,NETs与同步或异时性胃肠道及泌尿生殖系统SPMs高度相关。我们首次报告了一例纯神经内分泌乳腺癌(NEBC),其具有世界卫生组织(WHO)分类的所有形态学和表型神经内分泌特征(即梭形细胞、浆细胞样细胞、具有外周栅栏状倾向的大透明或黏液性印戒细胞的圆形实性巢,以及在超过50%的肿瘤细胞群体中神经内分泌标志物突触素和嗜铬粒蛋白免疫组化阳性),同时伴有同步性腹部非霍奇金淋巴瘤。在本研究中,我们回顾了NEBC的诊断、临床病理特征和组织发生学分析,并讨论了与该病例临床及解剖病理学管理相关的文献。这例先前未报告的同步性实性NEBC和腹部淋巴瘤病例,以及早期研究表明在NET患者的一个重要亚组中主要症状由SPMs引起,有力地支持了应谨慎将NETs视为索引肿瘤的观点。因此,强烈建议进行基于风险的临床病理随访并进行系统检查。

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