Síndrome de Zinner en paciente afecto de síndrome de Kallmann: rara asociacion de 2 malformaciones embrionarias

The relationship between renal agenesis and ipsilateral seminal cyst (Zinner syndrome) is a rare congenital anomaly. Its relationship with other embryonic malformations is even rarer. The case is presented of a 20-year-old male with Kallmann syndrome who was diagnosed with Zinner syndrome due to have bilateral testicular pain and dyspareunia of 3 years onset. After the laparoscopic excision was performed on the seminal vesicle affected, the patient became asymptomatic, maintaining normal ejaculation and correct erectile function.