Zinner syndrome incidentally diagnosed in a man with ureteropelvic junction stone and hydronephrosis: A case report

被引：0

作者：

Chiu, Tzu-Yu ^{[1
]}

Chen, Szu-Ju ^{[2
]}

Huang, Chun-Lin ^{[3
]}

Huang, Chi-Ping ^{[4
,5
]}

Chen, Wen-Chi ^{[4
,6
]}

机构：

[1] China Med Univ Hosp, Dept Med Educ, Taichung, Taiwan

[2] Taichung Vet Gen Hosp, Dept Urol, Taichung, Taiwan

[3] China Med Univ Hosp, Dept Radiol, Taichung, Taiwan

[4] China Med Univ Hosp, Dept Urol, Taichung, Taiwan

[5] Chinese Med Univ, Sch Chinese Med, Sch Med, Taichung, Taiwan

[6] China Med Univ, Sch Chinese Med, Grad Inst Integrated Med, Taichung, Taiwan

来源：

UROLOGY CASE REPORTS | 2025年 / 58卷

关键词：

Zinner syndrome; Polysplenia syndrome; Renal agenesis; Hydronephrosis;

D O I：

10.1016/j.eucr.2025.102930

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

Zinner syndrome is a congenital anomaly characterized by seminal vesicle cysts, ipsilateral renal agenesis, and ejaculatory duct obstruction possibly associated with infertility. Only 200 cases of Zinner syndrome have been reported since its discovery in 1914. We present the case of a 63-year-old man seeking treatment for a ureteropelvic junction stone causing severe hydronephrosis. After the patient's history and the computed tomography findings were reviewed, the diagnosis of Zinner syndrome was confirmed. The patient has been nearly asymptomatic and has had three children during his lifetime. Our case could serve as a reference for future diagnoses of this rare anomaly.

引用

页数：3

共 7 条

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