Ejaculatory duct cyst causing bilateral obstruction and subsequent infertility: A rare case report from Indonesia [PDF]
Radiology Case Reports, 2022 An ejaculatory duct cyst is a rare and challenging problem for a urologist. Diagnosing these cases may be difficult as prior case reports showed that the condition has various clinical presentations from asymptomatic to major complications, such as ...
Yudhistira Pradnyan Kloping +1 more
exaly +4 more sources
Azoospermia Due to Functional and Partial Ejaculatory Duct Obstruction: A Rare Case Report and Literature Review [PDF]
American Journal of Men's HealthEjaculatory duct obstruction (EDO) is a rare but treatable cause of male infertility. This case report describes a 28-year-old male with obstructive azoospermia. The patient came to our hospital after a fertility check-up revealed azoospermia.
Lihong Wang
exaly +3 more sources
Efficacy analysis of 26 cases of ejaculatory duct obstruction treated by prostatic utricle neck endoscopy [PDF]
Frontiers in Surgery, 2022 ObjectiveTo evaluate the safety and efficacy of transvesical incision in the treatment of ejaculatory duct obstruction.MethodsThe clinical data of 26 male infertile patients with ejaculatory duct obstruction were retrospectively analysed at the First ...
Kun-Long Lv +7 more
doaj +2 more sources
Ejaculatory duct reflux revealed by chronic scrotal swelling in an adult [PDF]
Urology Case Reports, 2022 Ejaculatory duct reflux is rare and few investigations have focused on this entity, which is usually described in children. This study reports a new case of unilateral ejaculatory reflux in a 32-year-old patient, with a history of urethroplasty at the ...
Selim Zaghbib +5 more
doaj +2 more sources
Ejaculatory Duct Obstruction in the Setting of an Ectopic Ureter [PDF]
Sexual Medicine, 2020 Introduction: A 17-year-old man was referred to a tertiary care urologist for hematuria, hematospermia, and testalgia. The patient had a history of right-sided renal dysgenesis at birth.
Joseph Shawn Smith, MD +1 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 UrologyBackground Zinner syndrome (ZS) is a congenital malformation characterized by a triad of mesonephric (Wolffian) duct dysplasia, first identified by Zinner in 1914.
Guixing Tang +6 more
doaj +2 more sources
Ejaculatory duct cyst mimicking post-TURP ejaculatory dysfunction: A diagnostic challenge in a patient with hemospermia and hypospermia [PDF]
Urology Case ReportsEjaculatory duct cysts are uncommon urological entities that can be difficult to diagnose after prostate surgery. We report a 60-year-old man who underwent TURP for a 65 g prostate and developed hemospermia and hypospermia six months later.
Youssef Maachi +6 more
doaj +2 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 ReportsIntroduction 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.
Taiju Hyuga +3 more
doaj +2 more sources
Ectopic ureter inserting into the ejaculatory duct: A case report [PDF]
Urology Case ReportsA 44-year-old man presented with bilateral flank pain, dysuria, and incomplete bladder emptying. Evaluation demonstrated a non-functioning atrophic left kidney, a markedly dilated tortuous ureter, and an ectopic ureter inserting into the left ejaculatory
Iyad Mashhoor Hakeem +3 more
doaj +2 more sources
Robot-Assisted Radical Prostatectomy in a Patient With Zinner Syndrome: A Case Report. [PDF]
IJU Case RepABSTRACT Introduction Zinner syndrome is a rare congenital urogenital anomaly characterized by seminal vesicle cysts, ejaculatory duct obstruction, and ipsilateral renal agenesis. Surgical treatment for prostate cancer in this setting has been reported in only 2 previous cases.
Yatsuda J +9 more
europepmc +2 more sources