Results 11 to 20 of about 1,146,359 (126)
Imaging in Zinner Syndrome, A Case Series: The Wolf in Sheep's Clothing. [PDF]
Urol Case RepZinner syndrome is a rare congenital malformation of the Wolffian duct with seminal vesicle cyst, ipsilateral renal agenesis and ejaculatory duct obstruction, seen in less than 0.002 % of the male population.
Pramod V, Sanjay SC, Tanuj Sai Kumar S.
europepmc +3 more sources
Overcoming the challenge of high surgical risk: Minimally invasive aspiration for Zinner syndrome in a geriatric patient with severe coronary artery disease. [PDF]
Radiol Case RepZinner syndrome is a rare congenital anomaly characterized by seminal vesicle cysts, ipsilateral renal agenesis, and ejaculatory duct obstruction, potentially leading to male infertility.
Cheng S +4 more
europepmc +3 more sources
Zinner syndrome presenting with intermittent scrotal pain in a young man
Radiology Case Reports, 2018 Congenital malformations of the seminal vesicle are uncommon, and most of them are cystic malformations. If an insult occurs during the first trimester of gestation, the embryogenesis of the kidney, ureter, seminal vesicle, and vas deferens could be ...
Sofia Florim +2 more
exaly +4 more sources
A Young Boy with Renal Agenesis and Ectopic Seminal Vesicle: Zinner Syndrome
Journal of Urological Surgery, 2023 Zinner syndrome is a rare disorder, and it is associated with unilateral renal agenesis, ipsilateral ejaculatory duct atresia (obstruction), and cystic dilatation of the ipsilateral seminal vesicle.
Ahmet Yasin Yitik +2 more
doaj +2 more sources
Zinner Syndrome: Case Series and Literature Review
Архивъ внутренней медицины, 2023 Zinner syndrome is a rare congenital anomaly of the mesonephric duct, characterized by a triad of symptoms: seminal vesicle cysts, ipsilateral renal agenesis and ejaculatory duct obstruction.
D. A. Kushnerova +3 more
doaj +2 more sources
European Journal of Case Reports in Internal Medicine, 2021 Zinner syndrome is a developmental anomaly of the urogenital tract. This condition is defined by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction. The syndrome is due to malformation of
Abakar Djidda +5 more
doaj +2 more sources
A rare variant of zinner syndrome with ejaculatory duct cyst: case report and challenges in diagnosis and management. [PDF]
BMC UrolBackground Zinner syndrome (ZS) is a congenital malformation characterized by a triad of mesonephric (Wolffian) duct dysplasia, first identified by Zinner in 1914.
Tang G +6 more
europepmc +3 more sources
Zinner syndrome: a case report and literature review [PDF]
Xin yixueObjective To investigate the key issues of clinical diagnosis and treatment of Zinner syndrome and reduce the misdiagnosis rate. Methods Clinical data of 1 case of Zinner syndrome were retrospectively analyzed. Zinner syndrome cases presenting hematuria，
YANG Yanmeng, ZHANG Feng, TANG Yanlong, BI Xiaoyang
doaj +3 more sources
Egyptian Journal of Radiology and Nuclear Medicine, 2023 Background Zinner syndrome is a rare Wolffian duct anomaly presenting as a triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction.
Dixit Varma
exaly +2 more sources
Zinner Syndrome—A Rare Cause of Recurrent Epididymitis and Infertility
Clinics and Practice, 2021 Zinner syndrome (ZS) is a rare disorder that affects only men. It is characterized by a triad of abnormalities, including unilateral renal agenesis, ipsilateral seminal vesicle cysts, and atresia of the ejaculatory tract.
Magdalena Ostrowska +7 more
doaj +2 more sources