A Case of Congenital Megalourethra / 대한비뇨기과학회지
Korean Journal of Urology
;
: 218-221, 1995.
Article
Dans Coréen
| WPRIM
| ID: wpr-57239
ABSTRACT
Megalourethra is a rare congenital abnormaly characterized by severe dilatation of urethra, the disorder at first reported by Nesbitt in 1955. The scaphoid type is due to poor development of the corpus spongiosum, whereas in the more severe fusiform variety the corpora cavernosa also are affected. We present a case of congenital scaphoid megalourethra associated with acute renal failure, sepsis and grade IV bilateral vesicoureteral reflux. Initial management of this patient was vesicocutaneostomy and urethrocutaneostomy followed later by urethral reconstruction.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Urètre
/
Reflux vésico-urétéral
/
Sepsie
/
Dilatation
/
Atteinte rénale aigüe
Limites du sujet:
Humains
langue:
Coréen
Texte intégral:
Korean Journal of Urology
Année:
1995
Type:
Article
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