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Abstract：
Zinner syndrome (ZS) is a highly uncommon congenital or developmental urogenital anomaly characterized by the triumvirate of unilateral renal agenesis or dysplasia, ipsilateral ejaculatory duct obstruction, and ipsilateral seminal vesicle cyst. We present three cases of ZS in a 21-year-old male, a 20-year-old male, and a 24-year-old male. The diagnostic evaluation revealed unilateral renal agenesis associated with hypertrophy of the ipsilateral seminal vesicle with cystic changes on investigation by ultrasonography (USG), computed tomography (CT), and magnetic resonance imaging (MRI). The patients underwent surgical management, resulting in symptom resolution and enhanced quality of life. This case report highlights the diagnostic challenges, management options, and long-term outcomes for patients with ZS.
摘要：
Zinner综合征（ZS）是一种非常罕见的先天性或发育性泌尿生殖系统异常，其特征是单侧肾脏发育不全或发育不良。同侧射精管阻塞,和同侧精囊囊肿。我们介绍了一名21岁男性的三例ZS，一个20岁的男性,还有一个24岁的男性.诊断评估显示，单侧肾发育不全与同侧精囊肥大相关，并通过超声检查（USG）进行囊性改变，计算机断层扫描（CT），磁共振成像（MRI）。患者接受了手术治疗，导致症状解决和提高生活质量。这份病例报告强调了诊断挑战，管理选项，以及ZS患者的长期结局。
