Zinner's syndrome: Case report of a rare maldevelopment in the male genitourinary tract

被引：3

作者：

Almuhanna, Ahmed M. ^{[1
]}

Alsuhaibani, Shaheed ^{[2
]}

Almesned, Razan ^{[3
]}

Almatar, Ashraf ^{[4
]}

Alali, Hamed ^{[4
]}

机构：

[1] King Fahad Hosp, Urol Dept, Al Hasa, Saudi Arabia

[2] Imam Abdulrahman Bin Faisal Univ, King Fahad Hosp, Urol Dept, Dammam, Saudi Arabia

[3] King Faisal Specials Hosp, Urol Dept, Riyadh, Saudi Arabia

[4] King Fahad Specials Hosp, Urol Dept, Dammam, Saudi Arabia

来源：

UROLOGY CASE REPORTS | 2021年 / 39卷

关键词：

Infertility; Zinner syndrome; Pregnancy; Case report;

D O I：

10.1016/j.eucr.2021.101839

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 rare congenital malformation of the urogenital tract. It is due anomaly in the developmental of Wolffian duct. Zinner syndrome comprises triad of seminal vesicle cyst, unilateral renal agenesis and ipsilateral ejaculatory duct obstruction. It is frequently associated with infertility. Herein we are highlighting a case of a 35 years-old male, a father of 4 biological children who presented to our clinic due to right hemiscrotal pain, associated with post ejaculation pain.

引用

页数：2

共 5 条

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