Unusual variant of inverted Y ureteral duplication with an ipsilateral seminal vesicle cyst and renal dysgenesis.
作者信息
Hajji F, Hammoune N, Miloudi M, Belasri S
机构信息
Third Military Hospital , Laayoune , Morocco.
Mohammed V Military Hospital , Rabat , Morocco.
出版信息
Ann R Coll Surg Engl. 2017 Jan;99(1):e19-e21. doi: 10.1308/rcsann.2016.0281. Epub 2016 Sep 23.
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.
摘要
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Unusual variant of inverted Y ureteral duplication with an ipsilateral seminal vesicle cyst and renal dysgenesis.
Ann R Coll Surg Engl. 2017 Jan;99(1):e19-e21. doi: 10.1308/rcsann.2016.0281. Epub 2016 Sep 23.
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