Case Of Seminal Vesicle Cyst Research Articles

A case of seminal vesicle cyst associated with ipsilateral renal agenesis diagnosed during an investigation of urinary incontinence

Seminal vesicle cysts are rare and usually associated with ipsilateral renal agenesis. The diagnosis of seminal vesicle cysts may be delayed or missed because of the non-specific symptoms of this condition. In this study, we aimed to discuss the diagnosis and treatment of a left seminal vesicle cyst that was associated ipsilateral agenesis in a 24-year-old patient who presented to our outpatient department with urinary incontinence. Ultrasonography and magnetic resonance imaging revealed a seminal vesicle cyst measuring 40×45 mm in diameter. Although the patient's symptoms were relieved with cyst aspiration via transrectal ultrasonography, the symptoms recurred 6 months later.

A Case of Seminal Vesicle Cyst Accompanied with Ipsilateral Renal Agenesis in an Infant

A Case of Seminal Vesicle Cyst Accompanied with Ipsilateral Renal Agenesis in an Infant

A Case of Seminal Vesicle Cyst Associated with Ipsilateral Renal Agenesis Diagnosed during an Investigation of Perineal Pain

A 38-year-old man was referred to our hospital with perineal and micturition pain. Transrectal ultrasound (TRUS) revealed a cystic mass in the outer prostate. Pelvic cyst and left renal agenesis were confirmed by magnetic resonance imaging (MRI) and computerized tomography (CT), and we diagnosed seminal vesicle cyst. The symptoms have since subsided, the possibility of sterility has been ruled out, and the patient is showing good improvement.

Quiste de vesícula seminal con agenesia renal asociado a malformaciones vasculares: Presentación de un caso

We report a case of seminal vesicle cyst with ipsilateral renal agenesis associated wit abnormalities of the abdominal great vessels, not described previously in the bibliography.33 year-old-male with history of abdominal pain and fever. This case was evaluated by ultrasound, IV urography, CT scan and MRI. RESULTS/CONCLUSIONS. Congenital cystic disease of the seminal vesicle is an uncommon disorder. It is associated with genitourinary anomalies, often renal agenesis, and even anomalies of the lower spine. However, anomalies of the abdominal great vessels have not been described previously. CT scan provided excellent demonstration of associated anomalies.

Endoscopic Management of Seminal-Vesical Cyst with Right Renal Agenesis Causing Acute Urinary Retention: Case Report

Seminal-vesicle cysts associated with renal agenesis are rare congenital or acquired lesions. We report a case of seminal-vesicle cyst causing urinary retention in a young patient with right renal agenesis who was treated successfully with transurethral unroofing. Magnetic resonance imaging aided us in making the conclusive diagnosis without the need for any invasive investigations.

Ultrasonographic and Computed Tomographic Diagnosis of Seminal Vesicle Cyst Associated with Ipsilateral Renal Agenesis: A Case Report

A rare case of seminal vesicle cyst associated with ipsilateral renal agenesis is reported. The role of ultrasonography and computed tomography in diagnosis and management is discussed. Congenital malformations of the seminal vesicle are most uncommon and most of them are cystic malformation. Approximately two thirds of them are associated with ipsilateral renal agenesis, since both the ureteral bud and seminal vesicle originate from the mesonephric duct. These were first described by Zinner in 1914 and nearly 120 cases had been reported till 1993. Most patients with this anomaly are asymptomatic or present during early adulthood with non-specific symptoms such as prostatism, urinary urgency, dysuria, painful ejaculation and perineal discomfort. Usually the cysts are 5.0cm or less in diameter and are either a symptomatic or present during early adulthood with symptoms such as urgency, burning, haematuria and hypogastric pain mainly after coitus. Less frequently cysts larger than 8-10 cm occur and such giant cysts can result in colon or bladder obstruction with palpation of mass per rectum. Recent advances in imaging techniques allow a better visualization of the prostate and surrounding structures. The application of transrectal ultrasonography has assumed a significant role in the management of these lesions. There have been few reports of the usefulness of computed tomography (CT) scan in such cases. In this case report, we insist that non-invasive imaging with ultrasonography and CT scan would be sufficient to diagnose case of seminal vesicle cyst associated with renal agenesis for management.

Difficult Urethral Catheterization due to Ectopic Ureter: an Unusual Presentation of Ureteral Ectopia in a Man

We report the unusual presentation of an ectopic ureter in a man with a solitary kidney. The presenting symptom was the inability to place a Foley catheter into the bladder because of preferential passage into the ectopic ureteral opening in the prostatic urethra. Flexible cystoscopy was helpful in diagnosis and management of the problem. The differential diagnosis of a difficult urethral catheterization should include occult congenital genitourinary anomalies.

Seminal vesicle cyst and ipsilateral renal agenesis

A case of seminal vesicle cyst with ipsilateral agenesis is presented. The embryologic events, clinical symptoms, and diagnosis are discussed, emphasizing the value of sonography and computer tomography in identifying the cyst. Surgical resection is the treatment of choice.

1 case of seminal vesicle cyst

1 case of seminal vesicle cyst

Seminal vesicle cyst containing mesonephroid tumor.

Abstract A case of seminal vesicle cyst containing mesonephroid tumor is reported. The radio-and pathologic features and the management of this unusual entity are described.

Seminal vesicle cyst and ipsilateral renal agenesis

A case of seminal vesicle cyst and ipsilateral renal agenesis is presented, the literature summarized, the embryology reviewed, and the differential diagnosis discussed. Our reasons for surgical therapy are stated.

Vasovesiculography: cyst of the seminal vesicle associated with agenesis of the ipsilateral kidney.

Abstract The authors present a case of seminal vesicle cyst associated with agenesis of the ipsilateral kidney. Various diagnostic methods are discussed. The authors believe that vasovesiculography offers the best approach to demonstrating the cyst. Differential diagnosis includes cysts of the wolffian duct which are usually larger, midline, and do not contain spermatozoa.

Urogenital malformation with cyst of the seminal vesicle, ipsilateral dilated ureter, and renal agenesis. Report of a case and review of the literature.

A case of seminal vesicle cyst, ipsilateral dilated ureter and renal agenesis is reported. The findings during the operation revealed a probable ectopic termination of the ureter into the seminal vesicle cyst. This uro-genital malformation is explained as a developmental failure in the same mesodermal region. The importance of complete urological examination is stressed when an otherwise healthy, young man gets vague uro-genital symptoms. The incidental finding of renal agenesis also should lead to supplementary investigations, by which other uro-genital malformations may be found.