A Case of Congenital Megalourethra / 대한비뇨기과학회지
Korean Journal of Urology
;
: 218-221, 1995.
Article
in Korean
| 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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Urethra
/
Vesico-Ureteral Reflux
/
Sepsis
/
Dilatation
/
Acute Kidney Injury
Limits:
Humans
Language:
Korean
Journal:
Korean Journal of Urology
Year:
1995
Type:
Article
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