Results 11 to 20 of about 2,430,707 (156)

Zinner Syndrome: The Diagnosis and Management of a Rare Urogenital Malformation. [PDF]

Case Rep Radiol
This 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
Lau L, Patel KS, Santisi F, Germaine R, Jeph S.   +4 more
europepmc   +3 more sources

A Rare Variant of Zinner Syndrome Involving Ectopic Ureteral Implantation into the Seminal Vesicle Causing Recurrent Epididymitis. [PDF]

Case Rep Urol
Zinner syndrome is a rare congenital anomaly characterized by a triad of renal dysgenesis/agenesis, cysts in the ipsilateral seminal vesicle, and ejaculatory duct obstruction.
Zaliznyak M, Baer A, Trierweiler J, Landon T, Hamilton Z.   +4 more
europepmc   +3 more sources

A case with an ectopic ejaculatory duct opening into the bladder trigone in Zinner syndrome, congenital unilateral renal agenesis, and an ipsilateral seminal vesicle cyst. [PDF]

IJU Case Rep
This report describes a case with an ectopic ejaculatory duct opening into the bladder trigone in Zinner syndrome, congenital unilateral renal agenesis, and an ipsilateral seminal vesicle cyst.
Hyuga T, Tanabe K, Kubo T, Moriya K.
europepmc   +3 more sources

Zinner syndrome incidentally diagnosed in a man with ureteropelvic junction stone and hydronephrosis: A case report. [PDF]

Urol Case Rep
Zinner syndrome is a congenital anomaly characterized by seminal vesicle cysts, ipsilateral renal agenesis, and ejaculatory duct obstruction possibly associated with infertility. Only 200 cases of Zinner syndrome have been reported since its discovery in
Chiu TY, Chen SJ, Huang CL, Huang CP, Chen WC.   +4 more
europepmc   +2 more sources

Zinner syndrome: Case report and brief review of the literature. [PDF]

Radiol Case Rep
Zinner syndrome (ZS) is a rare congenital anomaly of the mesonephric (Wolffian) duct, classically defined by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction.
Knutsen KR, Sico R, Hailemichael E, Lombard C, Lakhani DA.   +4 more
europepmc   +2 more sources

Zinner Syndrome: Case report of atypical symptoms and literature. [PDF]

Urol Case Rep
Zinner Syndrome is a rare congenital anomaly of the urogenital tract, characterized by unilateral renal agenesis, ejaculatory duct obstruction and ipsilateral seminal vesicle cyst.
Acuña-Pacheco A, González-Rojas E, Aguilar-Ordaz PI, Rodelo-López JP, Bueno-Mendoza B, Hernández-Rivera I, Jungfermann-Guzman JR, Favela-Camacho JR.   +7 more
europepmc   +2 more sources

Management Strategies for Seminal Vesicle Cysts in Zinner Syndrome: Insights From Two Cases. [PDF]

Cureus
Zinner syndrome is a rare congenital malformation that affects the male genitourinary tract, characterized by a triad of unilateral renal agenesis, seminal vesicle cysts, and ejaculatory duct obstruction, and typically presents during the third or fourth
Yusuf F, Husain A, Sikafi Z, Alhasani S, N Hasan M.   +4 more
europepmc   +2 more sources

The Hidden Triad: Decoding Zinner Syndrome Through Computed Tomography Urography and Magnetic Resonance Imaging. [PDF]

Cureus
Zinner syndrome is an uncommon congenital anomaly involving the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction.
Narayan S, Kombde B, Komwad A.
europepmc   +2 more sources

Diagnosis of Zinner syndrome: A case of rare occurrence. [PDF]

Radiol Case Rep
Zinner syndrome is a rare congenital urinary condition, secondary to disruptions in the embryonic development process between the fourth and 13th week of pregnancy, particularly due to abnormalities in the development of the distal mesonephric duct.
Thinh ND, Lam VD, My NTL, Dung LT, The ND, Loc TQ.   +5 more
europepmc   +2 more sources

Robotic-assisted management of Zinner syndrome: a case report and review of the surgical approach. [PDF]

J Surg Case Rep
Zinner syndrome typically presents in young adulthood with nonspecific symptoms, making diagnosis challenging. A 21-year-old male presented with pelvic and lower abdominal pain.
Alsaikhan B, Alasker A, Nazer A, Alkhamees M, Alghafees M, Bin Moammar AA, Alferayan T, Alrashed M, Alohali AA, Almanie A.   +9 more
europepmc   +2 more sources