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Seminal Vesicle Cysts
Seminal vesicle cysts are congenital or acquired and usually develop secondary to obstruction of the seminal tract. In congenital cysts, consider Zinner syndrome, characterized by ipsilateral renal agenesis or renal dysplasia and obstruction of the ejaculatory duct. Another cause is autosomal dominant polycystic kidney disease (ADPKD). Important differential diagnoses include an ectopic ureter, Müllerian duct cyst, prostatic cyst, and ureterocele. MRI is the diagnostic modality of choice (Arora et al., 2007).
Treatment is necessary only in the presence of symptoms or infection. Percutaneous perineal cyst drainage with sclerotherapy is an option but carries a relevant risk of recurrence. For large cysts or recurrence, consider laparoscopic, robot-assisted, or open seminal vesiculectomy. In the case of an ectopic ureter, laparoscopic nephroureterectomy with seminal vesiculectomy is the most common treatment option because renal function is often absent.
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References
Arora, S. S.; Breiman, R. S.; Webb, E. M.; Westphalen, A. C.; Yeh, B. M. & Coakley, F. V.
CT and MRI of congenital anomalies of the seminal vesicles.
AJR Am J Roentgenol, 2007, 189, 130-135
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