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Robotic management of painful Zinner syndrome, case report and review of literature

Laura Demaeyer, Serge Holz, Didier Pamart, Steven Taylor, Michel Naudin

2020International Journal of Surgery Case Reports15 citationsDOIOpen Access PDF

Abstract

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.

Topics & Concepts

MedicineAsymptomaticCystSeminal vesicleSurgeryLaparoscopyRenal agenesisAgenesisProstateKidneyInternal medicineCancerUrologic and reproductive health conditionsProstate Cancer Diagnosis and TreatmentTesticular diseases and treatments
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