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Annals of Pediatric Surgery. 2006; 2 (1): 50-52
in English | IMEMR | ID: emr-75934

ABSTRACT

Congenital ceco-vesical fistula [CCVF] associated with high anorectal malformation was not described before. The only described case in 1972 was associated with total colonic atresia which are not the case. We report a case of CCVF associated with a blind ended distal colon in a 50-day old male presented with high imperforate anus faecalurea, and epididymo -orchitis of the left testis. The bladder was separated from the cecum followed by abdomino-perineal pull-through of the colon. The relevant literature is reviewed, and the diagnostic modalities and management are discussed


Subject(s)
Humans , Male , Urinary Bladder Fistula/diagnosis , Urinary Bladder Fistula/surgery , Congenital Abnormalities/congenital , Colonic Diseases/congenital , Anus, Imperforate , Orchitis , Ultrasonography
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