Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, USA.
Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, USA; Department of Pathology and Laboratory Medicine, Weill Medical College of Cornell University, New York, NY, USA.
Ann Diagn Pathol. 2019 Oct;42:48-58. doi: 10.1016/j.anndiagpath.2019.06.009. Epub 2019 Jun 21.
Primary neuroendocrine tumors of the genitourinary tract are rare and are comprised of a heterogeneous group of neoplasms. These include paraganglioma, well-differentiated neuroendocrine tumors or carcinoid tumors, small-cell neuroendocrine carcinoma, and large-cell neuroendocrine carcinoma. Personal experiences, in addition to the findings of an extensive literature search for pertinent publications, were used to compile the epidemiological data, clinical information, histopathological features, prognostic factors, and therapeutic approaches. We also include molecular alterations and targeted treatments of the various neuroendocrine tumors of the genitourinary tract.
泌尿生殖系统原发性神经内分泌肿瘤较为罕见,由一组异质性肿瘤组成。这些肿瘤包括副神经节瘤、分化良好的神经内分泌肿瘤或类癌、小细胞神经内分泌癌和大细胞神经内分泌癌。除了广泛搜索相关文献外,我们还结合个人经验来编译流行病学数据、临床信息、组织病理学特征、预后因素和治疗方法。此外,我们还介绍了泌尿生殖系统各种神经内分泌肿瘤的分子改变和靶向治疗。