Zacharouli Konstantina, Vageli Dimitra P, Koukoulis George K, Ioannou Maria
Department of Pathology, Faculty of Medicine, School of Health Sciences, University of Thessaly, Biopolis, 41500 Larissa, Greece.
Mol Clin Oncol. 2022 Mar;16(3):67. doi: 10.3892/mco.2022.2500. Epub 2022 Jan 20.
Prostate cancer is one of the most commonly diagnosed malignancies in men. Most of these tumors are adenocarcinomas. Plasmacytoid is a rare variant of adenocarcinoma described by previous studies in the genitourinary system and is characterized by the plasmacytoid appearance of tumor cells with abundant cytoplasm and abnormally placed hyperchromatic nuclei. However, to the best of our knowledge, plasmacytoid adenocarcinoma has rarely been described in the prostate. This report describes a new case of plasmacytoid adenocarcinoma of the prostate diagnosed by biopsy and summarizes the known literature on plasmacytoid features in the genitourinary system. A 62-year-old male patient presented to the hospital with urinary retention, hematuria, weakness and weight loss. The digital rectal examination revealed an irregular enlargement. Laboratory findings showed elevated levels of prostate specific antigen (PSA; 43.6 ng/ml). Transrectal ultrasound showed invasion of the right seminal vesicle. Prostate tumor core biopsies were collected and sent for diagnosis. Histological examination revealed a high-grade prostatic adenocarcinoma Gleason score of 5+5 (total score 10). The tumor cells had a plasmacytoid appearance with abundant cytoplasm and abnormally placed hyperchromatic nuclei. The immunohistochemical phenotype was characterized by abundant positivity for cytokeratin (CK)AE1/AE3 and PSA. By contrast, tumor cells were negative for p63, CK 34BE12 and GATA binding protein 3 (urothelial markers), synaptophysin (neuroendocrine marker). Tumor cells were also negative for E-cadherin, which is particularly indicative of alterations. To the best of our knowledge, this is the first description of a plasmacytoid adenocarcinoma of the prostate diagnosed by biopsy, showing an irregular immunophenotype that may indicate somatic alterations. The presentation of a novel rare variant of prostatic carcinoma that differs from other neoplasms of the genitourinary system may contribute to an improved understanding of this uncommonly found histological pattern that may also be mandatory due to the clinical and prognostic implications of this diagnosis.
前列腺癌是男性中最常被诊断出的恶性肿瘤之一。这些肿瘤大多是腺癌。浆细胞样是先前在泌尿生殖系统研究中描述的一种罕见的腺癌变体,其特征是肿瘤细胞具有浆细胞样外观,细胞质丰富,核深染且位置异常。然而,据我们所知,前列腺中很少描述浆细胞样腺癌。本报告描述了一例经活检诊断的前列腺浆细胞样腺癌新病例,并总结了泌尿生殖系统中浆细胞样特征的已知文献。一名62岁男性患者因尿潴留、血尿、虚弱和体重减轻入院。直肠指检发现前列腺不规则增大。实验室检查结果显示前列腺特异性抗原(PSA)水平升高(43.6 ng/ml)。经直肠超声显示右侧精囊受侵。采集前列腺肿瘤核心活检组织送检。组织学检查显示为高级别前列腺腺癌,Gleason评分为5+5(总分10分)。肿瘤细胞具有浆细胞样外观,细胞质丰富,核深染且位置异常。免疫组化表型的特征是细胞角蛋白(CK)AE1/AE3和PSA呈强阳性。相比之下,肿瘤细胞对p63、CK 34BE12和GATA结合蛋白3(尿路上皮标志物)、突触素(神经内分泌标志物)呈阴性。肿瘤细胞对E-钙黏蛋白也呈阴性,这特别提示有改变。据我们所知,这是首例经活检诊断的前列腺浆细胞样腺癌的描述,显示出不规则的免疫表型,可能提示体细胞改变。一种与泌尿生殖系统其他肿瘤不同的新型罕见前列腺癌变体的出现,可能有助于更好地理解这种不常见的组织学模式,由于该诊断的临床和预后意义,这也可能是必要的。