Surgical treatment of Zinner syndrome


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Resumo

Zinner’s syndrome (SC) is a rare congenital disease characterized by ejaculatory duct obstruction, seminal vesicle cyst in combination with ipsilateral renal agenesis. This syndrome is due to development arrest of the Wolffian duct (mesonephros). Before the onset of sexual activity, the disease is asymptomatic. The main symptoms are nonspecific, including dysuria, urinary frequency, perineal and scrotal pain after ejaculation. A clinical case with the presentation of our own experience of surgical robot-assisted treatment of a patient with Zinner’s syndrome is presented in the article.

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Sobre autores

A. Kamalov

Moscow State University by Lomonosov; Medical Scientific and Educational Center of Lomonosov Moscow State University

urologist, Academician of the RAS, Ph.D., MD, professor, Head of the Department of Urology and Andrology, Faculty of Fundamental Medicine

V. Karpov

Moscow State University by Lomonosov; Medical Scientific and Educational Center of Lomonosov Moscow State University; GBUZ “GKB №31” of Moscow Healthcare Department

urologist, Honored Physician of the Russian Federation, Ph.D., associate professor at the Department of Urology and Andrology, Faculty of Fundamental Medicine

A. Pshihachev

Medical Scientific and Educational Center of Lomonosov Moscow State University; GBUZ “GKB №31” of Moscow Healthcare Department

urologist, Ph.D., MD, Department of Urology and Andrology, Faculty of Fundamental Medicine

I. Andreytsev

GBUZ “GKB №31” of Moscow Healthcare Department

surgeon, Ph.D., MD, Head of the Surgical Department No1 of

T. Takhirzade

GBUZ “GKB №31” of Moscow Healthcare Department

urologist, Head of the Department of Urology

M. Ekhoyan

GBUZ “GKB №31” of Moscow Healthcare Department

urologist

Z. Gevorkyan

Moscow State University by Lomonosov

resident at the Department of Urology and Andrology, Faculty of Fundamental Medicine

Bibliografia

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