V.P. Stus, N.N. Moiseenko, O.N. Volik, N.V. Dubovskaya, S.V. Ponomar, V.G. Kononenko

The experience and the results of treatment Zinner‘s syndrome (case report)

Development of the urinary and reproductive systems are interconnected. Laying and formation of the urogenital system passes difficult metamorphosis. There are three generation excretory organs: pronephros, primary kidney (mesonephros) and final kidney at the stage of embryogenesis. Infringement of the formation and development of mesonephros and its duct (Wolffian duct) in the embryo male leads to the formation of rare congenital malformations - pentad of mesonephros duct and Zinner‘s syndrome.

Zinner‘s syndrome is characterized unilateral renal aplasia, seminal vesicle cyst, obstruction of the vas deferens. Тhe syndrome manifests during peak sexual and reproductive activity of males. Specific symptoms of this disease does not exist. Patients complain of pelvic pain, pain in the perineum, dysuric disorders, blood in the urine and semen, infertility. The article presents a clinical case of a patient with the Zinner‘s syndrome. Diagnosis was based on complaints, medical history, ultrasound data kidney and pelvic organs. On the background of conservative therapy was achieved a positive treatment outcome.