Seminal vesicle cyst

Changed by Rohit Sharma , 25 Dec 2018

Updates to Article Attributes

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Seminal vesicle cysts can be congenital or acquired.

Congenital

Epidemiology

ItAge of presentation of congenital cysts is during the presenceperiod of greatest reproductive activity i.e in second and third decades of life, while acquired cysts withinare most often seen in the seminal vesicles since birthelderly age group.

Clinical presentation

Smaller cysts may be detected incidentally. It is seen rarely and occurs probably due to an obstruction atIn symptomatic patients, the junction of the seminal vesicle and ejaculatory duct. It is associated with many other urogenital anomalies:

  • renal agenesis or dysgenesis 1
  • ectopic insertion of ureter into seminal vesicleusual presenting features include perineal pain, ductus deferensabdominal pain, ejaculatory duct or prostatic urethra
  • ductus deferens agenesis
Acquired

This occurs secondary to the obstructionpain, dysuria, haematuria, increased frequency of the seminal vesicle causing cystic dilatation. 

infertility.

Pathology

Aetiology
Congenital

Congenital cysts occur due to insufficient drainage as a result of atresia of the ejaculatory ducts causing distension of seminal vesicles and further leading to the formation of a cyst. They usually become symptomatic in young adulthood due to the accumulation of secretions. These cysts are mostly unilateral with no predilection for the side of involvement

Congenital cysts are associated with many other urogenital anomalies:

  • renal agenesis or dysgenesis 1
  • ectopic insertion of ureter into seminal vesicle, ductus deferens, ejaculatory duct or prostatic urethra
  • ductus deferens agenesis
  • Zinner syndrome
Acquired

Acquired cysts are seen most often secondary to prostatic infection or surgery causing scarring and finally obstruction of the drainage of secretions. This is seen most often bilaterally.

Associations

Clinical presentation

Age

  • chronic infection and scarring of presentation of congenital cysts is during the period of greatest reproductive activity i.e in 2nd and 3rd decades of life while acquired cysts are most often seen in the elderly age group. Smaller cysts  may be detected incidentally. In symptomatic patients, the usual presenting features include perineal pain, abdominal pain,seminal vesicle or ejaculatory pain, dysuria, haematuria, increased frequency of micturition, urinary tract infections and infertility.duct
  • prior prostate surgery
  • autosomal dominant polycystic kidney disease5
  • Radiographic features

    Seminal vesicles appear normal or enlarged in size with presence of cysts within. 

    Ultrasound

    These can be imaged by transabdominal ultrasound and are best evaluated by transrectal ultrasound. The cysts may be anechoic or may contain internal debris from haemorrhage or infection.

    CT 

    Larger cysts may be seen on CT. The cysts may be seen as well defined, low attenuation lesions or  thickthick and irregular walled cysts with hyperdense contents in cases of secondary haemorrhage or infection. These lesions are classically located in the retro-vesicular region and cephalic to prostate. The associated renal anomalies can be depicted well.

    MRI

    Best in differentiating cystic pelvic lesions. Abdominal and pelvic anatomy can also be assessed. Classical appearance of cysts is maintained with low T1 and high T2 weighted signal intensity. Some seminal vesicle cysts may have high T1 and T2 signals probably due to proteinaceous contents or haemorrhage.

    Treatment and prognosis

    Depending on the size of the seminal vesicle cyst, surgery may be done.

    Differential diagnosis

    Other causes of male pelvic cystic masses can be included as a differential diagnosis. 

    References changed:

    • 5. Danaci M, Akpolat T, Baştemir M et al. The prevalence of seminal vesicle cysts in autosomal dominant polycystic kidney disease. Nephrol Dial Transplant. 1998;13(11):2825-8. <a href="https://doi.org/10.1093/ndt/13.11.2825">doi:10.1093/ndt/13.11.2825</a>
    • 5. Wolfgang Dähnert. Radiology Review Manual. (2011) <a href="https://books.google.co.uk/books?vid=ISBN9781609139438">ISBN: 9781609139438</a><span class="ref_v4"></span>

    Cases and figures

    • Case 1: with renal agenesis
    • Case 2: Zinner syndrome with right ectopic ureter
    • Case 3: with ipsilateral renal agenesis
    • Case 4: right
    • Case 5
    :

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