CONGENITAL SEMINAL-VESICLE CYSTS AND IPSILATERAL RENAL AGENESIS - CLINICAL-FEATURES BASED ON 7 CASES

Citation
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
Citations number
22
Categorie Soggetti
Urology & Nephrology
Journal title
ISSN journal
00034401
Volume
31
Issue
4
Year of publication
1997
Pages
184 - 190
Database
ISI
SICI code
0003-4401(1997)31:4<184:CSCAIR>2.0.ZU;2-Y
Abstract
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.