Affiliation:
1. Third Military Hospital, Laayoune, Morocco
2. Mohammed V Military Hospital, Rabat, Morocco
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.
Publisher
Royal College of Surgeons of England
Cited by
5 articles.
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