Zinner’s syndrome: a case of diagnosis of a rare disease
https://doi.org/10.51922/2074-5044.2026.1.124
Abstract
The article describes a clinical case of diagnosis of Zinner’s syndrome. This is a rare congenital anomaly of the genitourinary system in men, characterized by renal agenesis, ipsilateral obstruction of the vas deferens and a cyst of the seminal vesicle. The frequency of occurrence is less than 0,005 %. The case of patient R., 49 years old, who has been observed since adolescence for a single right kidney, a ureterocele on the right. After an examination using ultrasound and radiation examination methods, fibrocystoscopy revealed Zinner’s syndrome. The authors present their own diagnostic results of this disease.
About the Authors
R. N. KurlenkoBelarus
A. N. Ryapolov
Belarus
I. V. Nagornov
Belarus
D. V. Zabelin
Belarus
A. A. Litvishko
Belarus
A. N. Polikashkin
Belarus
A. V. Rudenkova
Belarus
M. O. Safronov
Belarus
О. G. Nominat
Belarus
References
1. Ayvazyan, A. V., Voino-Yasenetsky, A. M. Malformations of the kidneys and ureters. Moscow, Nauka, 1988, pp. 13–23.
2. Afanasyev, Yu. I., Yurina, N. A., Vinnikov, Ya. A., Radostina A. I., Chentsov Yu. S. Histology, embryology, cytology. Textbook. Moscow: GEOTAR-Media, 2014, pp. 631–633.
3. Zinner’s syndrome: a series of cases and a review of the literature / D. A. Kushnerova, V. S. Tikhonova, I. A. Blokhin, A. P. Gonchar // Archive of Internal Medicine. – 2023. – № 5.
4. Zinner syndrome: a case of diagnosis of a rare pathology / D. A. Dobroserdov, M. P. Kuchinsky, N. A. Filatova, L. T. Nalgieva // Bulletin of Urology. – 2023. – № 3.
Review
For citations:
Kurlenko R.N., Ryapolov A.N., Nagornov I.V., Zabelin D.V., Litvishko A.A., Polikashkin A.N., Rudenkova A.V., Safronov M.O., Nominat О.G. Zinner’s syndrome: a case of diagnosis of a rare disease. Military Medicine. 2026;(1):124-128. (In Russ.) https://doi.org/10.51922/2074-5044.2026.1.124
JATS XML