International Journal of Surgery Case Reports · 2020 · 15 citations · 6 references
MedicineSurgeryUrologyFemale UrologyUrogenital SurgeryUrologic SurgeryCongenital Renal AnomaliesCongenital Urinary Tract AnomaliesSeminal Vesicle PathologyCongenital PathologyCongenital Renal AgenesisCongenital Seminal Vesicle AnomaliesEjaculatory Duct Obstruction SurgeryRobotic-assisted LaparoscopySeminal Vesicle AgenesisSeminal Vesicle CystsUnilateral Renal Agenesis
BACKGROUND: Zinner Syndrome is a congenital pathology due to an embryologic anomaly occurring between the 4th and 13th gestational week. This embryologic defect leads to unilateral renal agenesis, ipsilateral seminal vesicle cyst and ejaculatory duct obstruction. Most of the time patients are asymptomatic and do not need any treatment but for symptomatic cases, only surgical removal of the cyst and seminal vesicle are 100% effective. CASE: The case presented here is that of a healthy 33-year old man with symptomatic right seminal vesicle cyst and ipsilateral renal agenesis. First a conservative approach was attempted but each time the symptoms ended up reappearing. We decided to use robot-assisted laparoscopy to completely resect the cyst and the right seminal vesicle. There was no postoperative complication and the patient's symptoms improved immediately. After a 6 months follow-up the patient remains completely asymptomatic. CONCLUSION: Complete excision of the seminal vesicle cyst is the only 100% effective treatment option for symptomatic patients with Zinner syndrome. Minimally invasive approaches like conventional laparoscopy or robotic assisted laparoscopy are safe and effective and should currently be considered as the surgical gold standard.
6
Zinner’s syndrome: report of two cases and review of the literature
Amine Slaoui, Souhail Regragui, Abdelouahad Lasri et al. · Basic and Clinical Andrology · 2016 · 36 citations · Full text
Medicine, Gynecology, Urology +17
Murat Can Kiremit, Ömer Acar, Alan A. Sag et al. · Journal of Endourology Case Reports · 2018 · 12 citations · Full text