| Literature DB >> 27659383 |
F Hajji1, N Hammoune1, M Miloudi1, S Belasri2.
Abstract
Inverted Y malformation is a rare variant of ureteral duplication with a marked female predominance. We describe a case of inverted Y ureteral duplication with concurrent ectopic ureteral insertion into a seminal vesicle cyst, a ureterocoele and renal dysgenesis, which occurred in a 29-year-old man with lower urinary tract symptoms, haematospermia and postcoital discomfort. To our knowledge, this is the first reported case with this constellation of urogenital abnormalities.Entities:
Keywords: Inverted Y; Renal dysgenesis; Seminal vesicle cyst; Ureteral duplication
Mesh:
Year: 2016 PMID: 27659383 PMCID: PMC5392803 DOI: 10.1308/rcsann.2016.0281
Source DB: PubMed Journal: Ann R Coll Surg Engl ISSN: 0035-8843 Impact factor: 1.891