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 +2 more sources
Zinner Syndrome in a Young Male: A Case Report and Review of the Literature. [PDF]
CureusZinner syndrome is an extremely uncommon congenital anomaly of the male urogenital tract. It is attributed to an embryological anomaly that arises in the distal segment of the mesonephric or Wolffian duct.
Kummari S, Ranga M.
europepmc +2 more sources
Zinner syndrome unveiled: Ectopic ureter and seminal vesicle cyst leading to urinary dysfunction: A case report. [PDF]
Radiol Case RepZinner syndrome (ZS) is a rare congenital urological condition characterized by a triad of ipsilateral seminal vesicle cysts, unilateral renal agenesis, and ejaculatory duct obstruction, first described in 1914.
Sawaftah Z +9 more
europepmc +2 more sources
Challenging clinical presentation of Zinner syndrome. [PDF]
Radiol Case Rep, 2023 Le syndrome de Zinner est une malformation congénitale rare du canal mésonéphrique comprenant un kyste de la vésicule séminale, une agénésie rénale ipsilatérale et une obstruction du canal éjaculatoire. La présentation clinique varie en fonction des douleurs périnéales, de l'éjaculation douloureuse, de l'hématospermie et de l'infertilité.
Sada F +18 more
europepmc +4 more sources
Zinner syndrome - case report. [PDF]
Med Pharm Rep, 2021 We present the case of a 51-year-old male with Zinner syndrome, which is a rare disease, resulting from an abnormal evolution of the mesonephric (Wolffian) duct. It consists in cystic dilations of one seminal vesicle and/or ejaculatory duct and ipsilateral renal agenesis.
Militaru V +6 more
europepmc +3 more sources
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 +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
A rare variant of zinner syndrome with ejaculatory duct cyst: case report and challenges in diagnosis and management. [PDF]
BMC UrolZinner 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 +2 more sources
Zinner syndrome: A rare congenital cause of infertility. [PDF]
Radiol Case RepZinner syndrome is a rare congenital malformation characterized by cystic seminal vesicles and ejaculatory duct obstruction in association with ipsilateral renal agenesis. It appears to be frequently linked to infertility.
Boui M +10 more
europepmc +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