Results 41 to 50 of about 1,146,359 (126)

Zinner syndrome: A case report of rare urogenital anomaly

open access: yesJournal of Medical Ultrasound, 2022
Zinner Syndrome is a rare urogenital tract anomaly with unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ipsilateral ejaculatory duct obstruction.
Bibek Gurung   +3 more
doaj   +1 more source

Zinner syndrome – a rare radiological diagnosis in a young male presenting with recurrent dysuria

open access: yesJournal of Society of Surgeons of Nepal, 2021
Zinner syndrome is a rare congenital abnormality of the mesonephric (Wolffian) duct consisting of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ipsilateral ejaculatory duct obstruction.
Dinesh Chataut   +3 more
doaj   +3 more sources

A rare case of Zinner syndrome: Triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ejaculatory duct obstruction

open access: yesRadiology Case Reports, 2021
A rare triad of Wolffian duct anomaly known as Zinner syndrome includes unilateral renal agenesis with ipsilateral seminal vesicle cyst and ejaculatory duct obstruction. It is often diagnosed in third and fourth decades of life.
Prabhat Karki, MD   +2 more
doaj   +1 more source

Seminal Vesicle Infection of Zinner Syndrome Misdiagnosed for Neoplasm [PDF]

open access: yesUrogenital Tract Infection, 2020
Zinner syndrome is a rare Müllerian duct congenital anomaly representing unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction. A 16-year-patient presented with dysuria, nocturia, and enduring diffuse perineal pain
Young Joo Kim
doaj   +1 more source

Right-sided Zinner syndrome with a left side quadrupled ureter– a case report

open access: yesRadiology Case Reports, 2021
Zinner syndrome is a rare congenital anomaly of the genitourinary tract, consisting of ipsilateral renal agenesis, seminal vesicle cysts, and ejaculatory duct obstruction.
Naqibullah Foladi, MD   +1 more
doaj   +1 more source

Zinner syndrome: Two cases and review of the literature

open access: yes, 2021
Zinner syndrome (ZS) is a rare congenital malformation due to abnormal development of the urogenital tract. It is caused by a growth failure of the distal part of the Müllerian duct in early embryogenesis.
Totaro A.   +3 more
core   +1 more source

Incidental detection of Zinner syndrome in a patient with nonseminomatous germ cell tumor of testis

open access: yesUrology Annals, 2020
Zinner syndrome is a rare congenital abnormality occurring in males comprising a triad of unilateral renal agenesis, ipsilateral ejaculatory duct obstruction, and seminal vesicle cyst.
Jeevitesh Khoda   +2 more
doaj   +1 more source

Si?ndrome de Zinner: um relato de caso / Zinner syndrome: a case report [PDF]

open access: yes, 2021
INTRODUÇÃO:  síndrome de Zinner é uma malformação genitourinária congênita rara, caracterizada por uma tríade de anomalias composta por cisto de vesícula seminal, obstrução do ducto ejaculatório, e agenesia renal ipsilateral.
Silva, Haiana Coelho Rocha   +11 more
core   +1 more source

Seminal Vesicle Abscess Associated with Zinner Syndrome [PDF]

open access: yes, 2017
We report a case of seminal vesicle abscess associated with Zinner syndrome. A 26-year-old male was admitted to our hospital because of fever and right scrotal swelling.
竹澤, 健太郎   +8 more
core   +1 more source

Laparoscopic removal of congenital seminal vesicle cyst in a preadolescent male: A unique case report

open access: yesJournal of the Scientific Society, 2021
Zinner syndrome refers to the triad of ipsilateral renal agenesis, seminal vesicle cysts, and ejaculatory duct obstruction. Ipsilateral renal agenesis may be associated with seminal vesicle cysts in 70% of cases, but a remnant ureteral bud has been shown
G Ajay Kumar   +4 more
doaj   +1 more source

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