Abstract

*Nachid A., Safwate R., Moumen O., Kbirou A., Moataz A., Dakir M., Debbagh A. and Aboutaieb R.

ABSTRACT

Zinner syndrome is a rare congenital anomaly resulting from Wolffian duct maldevelopment and is characterized by the triad of ipsilateral renal agenesis, seminal vesicle cyst, and ejaculatory duct obstruction. It often remains asymptomatic and is incidentally discovered, but when symptomatic, it can present with pelvic discomfort, urinary symptoms, or infertility. We report the case of a 39-year-old male, father of three, who presented with intermittent hemospermia. Imaging confirmed the diagnosis of Zinner syndrome, revealing a right seminal vesicle cyst associated with ipsilateral renal agenesis.