Congenital Seminal Vesicle Cyst and Ipsilateral Renal Agenesis (Zinner Syndrome): A Rare Association and Its Evolution from Early Childhood to Adolescence

European Journal of Pediatric Surgery Reports
Aikaterini KanavakiSylviane Hanquinet

Abstract

Zinner syndrome, the association of congenital seminal vesicle cyst and ipsilateral renal agenesis, is more often reported in adults or older adolescents. We present a case of a boy, followed up in our hospital since birth for right renal agenesis who at the age of 4 years presented a right paravesical cyst on ultrasound. The cyst was initially considered as an ureterocele. The diagnosis of Zinner syndrome was made later, at the age of 15 years by ultrasound and magnetic resonance imaging; at that moment the cyst had increased in size and had changed in aspect. This malformation should be considered in the differential diagnosis of a pelvic cyst in male patients with renal agenesis.

Citations

Feb 15, 2019·Military Medical Research·Evangelos N SymeonidisMichail Papathanasiou
Apr 27, 2019·Frontiers in Pediatrics·Valentina CasciniPierluigi Lelli Chiesa
Nov 6, 2020·International Journal of Impotence Research·Aybike HofmannWolfgang H Roesch
Mar 26, 2021·Case Reports in Urology·Niall P KellyPadraig J Daly
Oct 16, 2018·The Indian Journal of Radiology & Imaging·Raj Bharatkumar Koticha

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