Results 31 to 40 of about 2,430,707 (156)

Case Report: Incidental finding of Zinner syndrome in an asymptomatic 53-year-old Palestinian male. [PDF]

Front Urol, 2023
Introduction Zinner syndrome (ZS) is a rare condition characterized by a triad of seminal vesicle cyst (SVC), ipsilateral ejaculatory duct obstruction, and ipsilateral renal agenesis.
Abu-Hilal LH, Barghouthi DI, Njoum Y, Obeid A, Alshawwa K, AbuKeshek T, Maree M.   +6 more
europepmc   +2 more sources

Zinner syndrome: A first case report from Ethiopia. [PDF]

Radiol Case Rep, 2023
A triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction has been called Zinner syndrome since its first description in 1914 by Zinner. It is a very rare congenital abnormality of the male genitourinary tract due to abnormal embryologic development of the Wolffian ducts. There have been several
Beyene E, Tadele E, Negassa M.
europepmc   +4 more sources

Zinner syndrome: a rare diagnosis in infancy. [PDF]

BMJ Case Rep, 2022
We present a case of Zinner syndrome (ZS), where we were fortunate to diagnose a child with this rare syndrome immediately after birth. Gross hydronephrosis was observed during the prenatal period on ultrasound, and further imaging after birth confirmed the presence of a multicystic dysplastic kidney and seminal vesicle cyst.
Rose JMO, Banthia R, Tamboli Z, Lal H.
europepmc   +3 more sources

Zinner Syndrome: A Rare Case Report

Journal of Urological Surgery
Over 200 cases of seminal vesicle cysts linked to ipsilateral renal agenesis have been reported in the literature, indicating Zinner syndrome. This condition occurs when the ureteric buds fail to meet the metanephros, leading to cystic dilatation in the ipsilateral seminal vesicle along with unilateral renal agenesis.
Gaurang R. Shah, Achint Bajpai, Husain Burhanpurwala   +2 more
openaire   +3 more sources

Zinner syndrome in pediatric patients: rare disease leading to challenging management. [PDF]

Front Pediatr
Introduction Zinner syndrome (ZS) is the association of seminal vesicle cysts, ipsilateral ejaculatory duct obstruction, and ipsilateral renal agenesis. This condition is very rare in children and both diagnosis and treatment may be challenging.
Adorisio O, Orazi C, Gregori LM, De Peppo F, Silveri M.   +4 more
europepmc   +2 more sources

Successful Laparoscopic Management of Zinner Syndrome in a Pediatric Patient.

J Indian Assoc Pediatr Surg
Zinner syndrome, a rare congenital anomaly affecting males, is characterized by atresia of the ejaculatory duct, seminal vesicle cysts, and ipsilateral renal agenesis.
Kulkarni K, Dhua AK, Goel P, Jain V, Yadav DK, Agarwala S, Kandasamy D.   +6 more
europepmc   +2 more sources

Zinner Syndrome with Papillary Neoplasm: A Rare Case Report.

J Indian Assoc Pediatr Surg, 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, ipsilateral seminal vesicle obstruction, and ipsilateral ejaculatory duct
Randhawa JS, Shankaran R, Nagamahendran R, Upadhye MA, Deepak H.   +4 more
europepmc   +4 more sources

Potential pharmacotherapy for Zinner syndrome. [PDF]

Transl Androl Urol, 2023
Takeshima T.
europepmc   +3 more sources

Editorial Comment on "Zinner Syndrome Presenting With Chronic Pelvic Pain and Ejaculatory Dysfunction" From Dr. Sourav and Dr. Tweheyo. [PDF]

IJU Case Rep
IJU Case Reports, Volume 8, Issue 4, Page 328-329, July 2025.
Sudan S, Ronald T.
europepmc   +2 more sources

Editorial Comment From Dr. Chelsea and Dr. Ranjana to Zinner Syndrome Presenting With Chronic Pelvic Pain and Ejaculatory Dysfunction. [PDF]

IJU Case Rep
IJU Case Reports, Volume 8, Issue 4, Page 326-327, July 2025.
Tafawa CR, Sah R.
europepmc   +2 more sources