University Health Network, Toronto, ON, Canada.
Hamad Medical Corporation, Doha, Qatar.
Histopathology. 2017 Dec;71(6):926-933. doi: 10.1111/his.13330. Epub 2017 Oct 6.
The current World Health Organization classification categorises high-grade neuroendocrine (NE) carcinomas of the prostate into small-cell and large-cell types. A distinct form of carcinoma showing synchronous dual exocrine and NE differentiation, termed amphicrine carcinoma, has been described at various other sites, primarily within the gastrointestinal tract. The aim of this study was to investigate the clinicopathological features of a series of metastatic prostate carcinoma (PCa) cases with amphicrine features.
Five cases of high-grade PCa showing an amphicrine immunohistochemical phenotype were prospectively collected. The serum prostate-specific antigen (PSA) level at diagnosis ranged from 38 ng/ml to 992 ng/ml (median 200 ng/ml). All five patients had metastatic disease, four at initial presentation. Microscopically, the tumours showed a solid/nested growth pattern composed of cells with amphophilic cytoplasm, vesicular nuclei, and macronucleoli. Morphological features of small-cell or large-cell NE carcinoma were absent. As compared with conventional high-grade PCa, the tumour cells showed a higher level of nuclear pleomorphism, brisk mitotic activity, and a high Ki67 proliferation index (median 50%). All cases showed immunohistochemical positivity for PSA, androgen receptor, and prostate-specific acid phosphatase, combined with diffuse or confluent/non-focal positivity for chromogranin-A and synaptophysin. Two hormone-naive cases showed a clinical response to androgen deprivation therapy.
This series highlights a previously undefined, clinically aggressive variant of PCa showing dual exocrine and NE differentiation, for which we are proposing the term PCa with amphicrine features. Increased recognition of these tumours may lead to a better understanding of their biology, and ultimately improve their clinical management.
目前世界卫生组织(WHO)分类将前列腺高级别神经内分泌(NE)癌分为小细胞和大细胞类型。在其他各种部位,主要是在胃肠道中,已经描述了一种具有同步外分泌和 NE 分化的独特癌形式,称为两性细胞癌。本研究旨在研究具有两性细胞特征的一系列转移性前列腺癌(PCa)病例的临床病理特征。
前瞻性收集了 5 例具有两性细胞免疫组织化学表型的高级别 PCa 病例。诊断时的血清前列腺特异性抗原(PSA)水平范围为 38 ng/ml 至 992 ng/ml(中位数 200 ng/ml)。所有 5 例患者均有转移性疾病,4 例在初次就诊时。显微镜下,肿瘤呈实性/巢状生长模式,由具有嗜碱性细胞质、泡状核和大核仁的细胞组成。无小细胞或大细胞 NE 癌的形态特征。与常规高级别 PCa 相比,肿瘤细胞具有更高水平的核多形性、活跃的有丝分裂活性和高 Ki67 增殖指数(中位数 50%)。所有病例均显示 PSA、雄激素受体和前列腺特异性酸性磷酸酶免疫组织化学阳性,结合弥漫性或连续/非局灶性染色阳性的嗜铬粒蛋白 A 和突触素。2 例激素初治病例对雄激素剥夺治疗有临床反应。
本系列研究强调了一种以前未定义的、具有临床侵袭性的 PCa 变体,其具有双重外分泌和 NE 分化,我们建议将其命名为具有两性细胞特征的 PCa。对这些肿瘤的认识增加可能会导致更好地了解其生物学特性,并最终改善其临床管理。