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Zinner’s syndrome. Clinical case
- Authors: Bokovoi S.P.1, Zverev Y.A.2, Perfileva O.V.2, Bobyleva M.N.2
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Affiliations:
- Northern State Medical University
- Arkhangelsk Regional Clinical Hospital
- Issue: Vol 13, No 1 (2023)
- Pages: 99-104
- Section: Сlinical observations
- URL: https://journals.eco-vector.com/uroved/article/view/321741
- DOI: https://doi.org/10.17816/uroved321741
- ID: 321741
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Abstract
Zinner’s syndrome refers to rare malformations and is characterized by a triad of signs - unilateral renal agenesis, obstruction of the vas deferens, and cystic transformation of the seminal vesicle. A description of a clinical case of Zinner’s syndrome with an atypical clinical picture is presented. This observation indicates the need for an in-depth examination of the genital organs in men with renal agenesis.
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About the authors
Sergey P. Bokovoi
Northern State Medical University
Email: sepalbok@mail.ru
ORCID iD: 0000-0003-3800-4130
http://www.nsmu.ru/consult-policl/consult/urolog.php
MD, Cand. Sci. (Med.), assistant professor of the Department of Surgery, Course of Urology
Russian Federation, ArkhangelskYurii A. Zverev
Arkhangelsk Regional Clinical Hospital
Email: zverevya@aokb.ru
head of the Urological Division
Russian Federation, 292 Lomonosova av., Arhangelsk 163045Olga V. Perfileva
Arkhangelsk Regional Clinical Hospital
Email: sepalbok@mail.ru
urologist
Russian Federation, 292 Lomonosova av., Arhangelsk 163045Maria N. Bobyleva
Arkhangelsk Regional Clinical Hospital
Author for correspondence.
Email: bobylevamn@aokb.ru
urologist
Russian Federation, 292 Lomonosova av., Arhangelsk 163045References
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