Magnetic Resonance Imaging of Seminal Vesicle Cyst Associated with Ipsilateral Urinary Anomalies

Seminal vesicle cysts rarely cause symptoms. Data on long-term follow-up from childhood to adulthood are lacking. The study analyzed the magnetic resonance imaging (MRI) and follow-up results of this condition. From 1991 to 1996, seminal vesicle cyst was diagnosed in 13 boys (mean age, 12 years; ran...

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Veröffentlicht in:Journal of the Formosan Medical Association 2006, Vol.105 (2), p.125-131
Hauptverfasser: Chen, Huan-Wu, Huang, Sheng-Chau, Li, Yiu-Wah, Chen, Shyh-Jye, Sheih, Chung-Pin
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Sprache:eng
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Zusammenfassung:Seminal vesicle cysts rarely cause symptoms. Data on long-term follow-up from childhood to adulthood are lacking. The study analyzed the magnetic resonance imaging (MRI) and follow-up results of this condition. From 1991 to 1996, seminal vesicle cyst was diagnosed in 13 boys (mean age, 12 years; range, 7-15 years), six of whom had long-term follow-up data. The clinical symptoms and MRI findings at diagnosis and at follow-up were analyzed. The seminal vesicle cyst was on the right side in six patients and on the left in seven. The size varied, ranging from 1.0 × 1.3 × 1.4 to 4.4 × 3.1 × 3.6 cm. All showed high signal intensity on T2-weighted images but variable signal intensity on T1-weighted images. Associated urinary tract anomalies included renal anomalies (dysplasia in 2 patients, agenesis in 11), ectopic ureteral orifice (11), hydroureter (6), and vertebral anomalies (2). One of the six patients with follow-up had repeated urinary tract infection and underwent surgical resection of the cyst 8 years after the diagnosis. The other five had no symptoms during the follow-up period. Three of the six patients had repeat MRI after a median of 11 years, which showed slight cyst enlargement and increased T1-weighted signal intensity. Most seminal vesicle cysts were asymptomatic and did not change during long-term follow-up. MRI is a powerful tool for detecting seminal vesicle cysts and in delineating associated congenital anomalies of the urogenital tract.
ISSN:0929-6646
1876-0821
DOI:10.1016/S0929-6646(09)60333-8