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Zinner Syndrome: The Diagnosis and Management of a Rare Urogenital Malformation. [PDF]
Case Rep RadiolThis case highlights an atypical but important consideration in young males presenting with persistent gastrointestinal and/or genitourinary symptoms. Zinner syndrome (ZS) develops from embryologic maldevelopment of the distal mesonephric duct, resulting in ejaculatory duct atresia with consequent obstruction of the seminal vesicle and concomitant ...
Lau L +4 more
europepmc +2 more sources
Indian Journal of Urology, 2010 The present article reports a triad of right renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction (Zinner syndrome) in a 19-year boy who presented with urinary symptoms.
Nitin P Ghonge +2 more
doaj +2 more sources
A variant of Zinner syndrome with ectopic ureteral insertion into the seminal vesicle. [PDF]
Radiol Case RepZinner syndrome comprises a triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction, which can be accompanied by additional abnormalities of the genitourinary tract in some cases.
Al-Smair A +3 more
europepmc +2 more sources
European Journal of Pediatric Surgery Reports, 2015 Zinner syndrome, the association of congenital seminal vesicle cyst and ipsilateral renal agenesis, is more often reported in adults or older adolescents. We present a case of a boy, followed up in our hospital since birth for right renal agenesis who at
Aikaterini Kanavaki +3 more
doaj +2 more sources
Infected Pelvic Cyst: A Postoperative Complication in a Patient with Zinner Syndrome: A Case Report
Journal of Urological SurgeryZinner syndrome is a rare disorder characterized by congenital seminal vesicle cysts, multicystic dysplastic kidney, and ipsilateral upper urinary tract anomalies.
Erdem Orman +5 more
doaj +2 more sources
Zinner syndrome with contralateral hydronephrosis: A rare congenital condition. [PDF]
Urol Case RepZinner Syndrome (ZS) is a rare congenital genitourinary abnormality defined by seminal vesicle cysts, ejaculatory duct obstruction, and unilateral renal dysplasia or agenesis.
Shanholtzer A +3 more
europepmc +2 more sources
An unusual variant of Zinner syndrome with ureteral ectopia from an atrophied supernumerary kidney
Urology Case Reports, 2020 This case presents an unusual variation of Zinner syndrome with a patient found to have an ectopic ureteral insertion of the seminal vesicle from a supernumerary pelvic kidney and complete duplication of the ipsilateral, otherwise normal renal unit.
Lucas R Wiegand
exaly +3 more sources
The Association of Renal Agenesis and Ipsilateral Seminal Vesicle Cyst: Zinner Syndrome Case Report
Case Reports in Urology, 2019 Introduction. Zinner syndrome is a rare congenital malformation characterized by the association of an ipsilateral renal agenesis, ipsilateral seminal vesicle cyst, and ipsilateral ejaculatory duct obstruction.
Mishal AlArifi +2 more
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Zinner syndrome with papillary neoplasm: A rare case report
Journal of Indian Association of Pediatric Surgeons, 2022 One of the uncommon urogenital malformations in males, which presents late in the second or third decades of life, is the congenital malformation of the seminal vesicle. Zinner syndrome is a rare condition comprising a triad of unilateral renal agenesis,
Jaskiran S Randhawa +4 more
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Fistula-unexpected complication after rectal cancer surgery due to Zinner syndrome
Urology Case Reports, 2022 Zinner syndrome is an uncommon developmental defect of men's urogenital system, described as a triad of unilateral kidney underdevelopment, seminal vesicle cysts, and ejaculatory duct blockage.
Vestina Strakšytė, Augustina Gylienė
doaj +1 more source