Zinner syndrome with contralateral hydronephrosis: A rare congenital condition

被引:1
作者
Shanholtzer, Andrew [1 ]
Sidhom, Daniel A. [1 ]
Suson, Kristina D. [2 ]
Anderson, Barrett G. [1 ]
机构
[1] Detroit Med Ctr, Dept Urol, Detroit, MI 48201 USA
[2] Childrens Hosp Michigan, Dept Urol, Detroit, MI USA
来源
UROLOGY CASE REPORTS | 2024年 / 56卷
关键词
Zinner syndrome; Hydronephrosis; CYSTS;
D O I
10.1016/j.eucr.2024.102818
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 (ZS) is a rare congenital genitourinary abnormality defined by seminal vesicle cysts, ejaculatory duct obstruction, and unilateral renal dysplasia or agenesis. Patients can be asymptomatic, while others experience pain, urinary or ejaculatory symptoms and infertility. A patient that presented with painless gross hematuria was found to have a large pelvic cystic structure, an absent left kidney, multiple fluid collections in the region of the left seminal vesicle and right hydronephrosis. Hydronephrosis is atypical in ZS. This patient eventually developed right flank and pelvic pain treated with robotic-assisted laparoscopic excision of the pelvic cystic structure and extravesical ureteral reimplantation.
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页数:4
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