Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
7271486 | Revista Internacional de Andrología | 2016 | 4 Pages |
Abstract
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.
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Authors
Arturo DomÃnguez, José M. Abascal-Junquera, Jesús Muñoz-RodrÃguez, Josep M. Banús,