Robinson Alexandra S, Shkoukani Zakaria W, Khadr Rauf, Stevenson James, Abdulmajed Mohamed I
Department of Urology, Mersey and West Lancashire Teaching Hospitals NHS Trust, Liverpool, GBR.
Cureus. 2024 Nov 29;16(11):e74773. doi: 10.7759/cureus.74773. eCollection 2024 Nov.
Metastasis of prostate cancer to the testes is exceptionally rare. We report the case of a 67-year-old male with a 10-year history of high-risk prostate cancer, previously treated and currently in remission, who presented with left scrotal swelling. The swelling was clinically and radiologically diagnosed as a hydrocele and treated surgically. A postoperative localized infection complicated the hydrocele repair. Two years after the surgery, the patient presented with a reoccurrence of scrotal swelling, coinciding with an insignificant increase in serum prostate-specific antigen (PSA) levels from 0.4 ng/mL to 2.0 ng/mL. Furthermore, computed tomography (CT) imaging of the abdomen and pelvis demonstrated no suspicious masses and normal appearance of the underlying testes. However, repeat ultrasonography of the left testis revealed an irregular and diffusely heterogeneous testis with increased vascularity. Presuming these findings to be fibrotic scrotum following a hydrocele repair complicated with postoperative infection, a left inguinal orchidectomy was performed. Histopathological analysis revealed extensive infiltration of the testicular parenchyma by adenocarcinoma, characterized by cribriform glands, round nuclei, and prominent nucleoli. Immunohistochemical analysis revealed widespread positivity for PSA and moderate, patchy expression of NKX3.1. Additionally, there was focal, strong staining for chromogranin and synaptophysin. A collaborative evaluation by the multidisciplinary team involving urological surgeons, pathologists, and radiologists was crucial in reaching the final diagnosis of metastatic prostate adenocarcinoma to the testis. This case emphasizes the importance of maintaining a high suspicion for metastasis in prostate cancer patients, even when clinical or radiological findings are not prominent, as the diagnostic approach may not always follow a predictable course.
前列腺癌转移至睾丸极为罕见。我们报告一例67岁男性,有10年高危前列腺癌病史,此前接受过治疗且目前处于缓解期,现出现左侧阴囊肿胀。临床上和影像学上该肿胀被诊断为鞘膜积液并接受了手术治疗。鞘膜积液修复术后出现局部感染并发症。手术两年后,患者阴囊肿胀复发,同时血清前列腺特异性抗原(PSA)水平从0.4 ng/mL轻微升高至2.0 ng/mL。此外,腹部和盆腔的计算机断层扫描(CT)成像未显示可疑肿块,睾丸外观正常。然而,左侧睾丸的重复超声检查显示睾丸不规则且弥漫性不均匀,血管增多。鉴于这些发现被认为是鞘膜积液修复术后并发感染后的纤维化阴囊,遂进行了左侧腹股沟睾丸切除术。组织病理学分析显示腺癌广泛浸润睾丸实质,其特征为筛状腺体、圆形细胞核和明显的核仁。免疫组织化学分析显示PSA广泛阳性,NKX3.1呈中度、散在表达。此外,嗜铬粒蛋白和突触素呈局灶性强染色。由泌尿外科医生、病理学家和放射科医生组成的多学科团队进行的联合评估对于最终诊断为睾丸转移性前列腺腺癌至关重要。该病例强调了即使临床或影像学表现不明显,对前列腺癌患者的转移仍需高度怀疑的重要性,因为诊断方法可能并不总是遵循可预测的过程。