U. Humke et al., CONGENITAL SEMINAL-VESICLE CYSTS AND IPSILATERAL RENAL AGENESIS - CLINICAL-FEATURES BASED ON 7 CASES, Annales d'Urologie, 31(4), 1997, pp. 184-190
Seminal vesicle cysts with ureteral ectopy and ipsilateral renal agene
sis or dysplasia are rare congenital malformations. This study reports
7 consecutive cases in a single center and, for the first time in the
literature, reports long-term results on 5 cases. Patients were betwe
en the age of 15 and 57 years. The malformation was diagnosed in all c
ases with excretory urography, computed tomography, magnetic resonance
imaging and cystoscopy. 5 patients were followed after diagnosis for
26 to 119 months (mean 52 months). Only 2 of 7 patients primarily pres
ented with nonspecific lower urinary tract symptoms. One patient (15 y
ears old) showed significant enlargement of the cysts with compression
of the urinary bladder and signs of urinary incontinence 10 years aft
er primary diagnosis. The other 4 patients had no changes of their mal
formation, In conclusion, seminal vesicle cysts with ipsilateral renal
agenesis are now more frequently diagnosed because of the increasing
use of sectional imaging procedures. They are mostly asymptomatic and
their morphology does not change with time. These data support the con
cept of only treating symptomatic patients.