Suppr超能文献

低前列腺特异性抗原水平的罕见类型前列腺腺泡腺癌:两例多形性巨细胞腺癌的组织病理学报告

Unusual Type of Acinar Adenocarcinoma of the Prostate With Low PSA: A Histopathological Report of Two Cases of Pleomorphic Giant Cell Adenocarcinoma.

作者信息

Stoyanov George S, Kirilova Andrea, Naydenova Kristina, Popov Hristo

机构信息

Department of Pathology, Multiprofile Hospital for Active Treatment, Shumen, Bulgaria.

Laboratory of Cytopathology, Diagnostic and Consultative Center, Shumen, Bulgaria.

出版信息

Case Rep Oncol Med. 2025 Sep 9;2025:7658657. doi: 10.1155/crom/7658657. eCollection 2025.

Abstract

Prostate adenocarcinoma is among the leading malignant neoplastic processes in overall incidence and among the leaders of cancer-related deaths. Clinically, there is a higher risk of development in males over 50, and suspicion is increased in all cases of elevated prostate-specific antigen (PSA) levels. While the most common histologies are of conventional ductal and acinar prostatic adenocarcinoma, there are some exceedingly rare histological patterns and subtypes that vary from conventional carcinomas not only in their histological makeup but also in their presentation and aggressiveness. Herein, we report two cases of male patients aged 75 and 60 years who presented to our institution with the leading complaint of urinary retention and gross hematuria and concomitant hydronephrosis. In both patients, the PSA levels were within normal reference values. As such, they were scheduled for transurethral resection of the prostate, with histopathology of the resected specimens showing a pleomorphic tumor process with foci of pseudoacinar structures comprised of large atypical cells with large hyperchromic nuclei, some of which had a monstrous appearance, solid tumor cell aggregates, sheets, and single tumor cells invading the parenchyma, represented mainly by large tumor cells with macroanisokaryosis, nuclear hyperchromasia, and pronounced pleomorphism. Pleomorphic giant cell prostatic carcinomas rarely present with elevated PSA or specific imaging findings and are often diagnosed incidentally, further contributing to their rarity.

摘要

前列腺腺癌在总体发病率中位居主要恶性肿瘤之列,在癌症相关死亡原因中也名列前茅。临床上,50岁以上男性发病风险较高,前列腺特异性抗原(PSA)水平升高的所有病例中,患癌嫌疑都会增加。虽然最常见的组织学类型是传统的导管和腺泡前列腺腺癌,但也有一些极其罕见的组织学模式和亚型,它们不仅在组织学构成上与传统癌不同,在临床表现和侵袭性方面也有所差异。在此,我们报告两例男性患者,年龄分别为75岁和60岁,他们因尿潴留、肉眼血尿伴肾积水为主诉前来我院就诊。两名患者的PSA水平均在正常参考值范围内。因此,他们被安排进行经尿道前列腺切除术,切除标本的组织病理学检查显示为多形性肿瘤病变,有假腺泡结构灶,由具有大的非典型细胞核的大细胞组成,其中一些细胞形态怪异,还有实性肿瘤细胞聚集体、细胞片以及侵袭实质的单个肿瘤细胞,主要表现为具有核大小不均、核深染和明显多形性的大肿瘤细胞。多形性巨细胞前列腺癌很少表现为PSA升高或特定的影像学表现,且常为偶然诊断,这进一步导致了它们的罕见性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f1/12440663/2cc5468a079d/CRIONM2025-7658657.001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验