A Cloacal Exstrophy Variant Associated with Hindgut Duplication
Journal of the Korean Association of Pediatric Surgeons
;
: 190-194, 1995.
Artigo
em Coreano
| WPRIM
| ID: wpr-740633
ABSTRACT
Diphallus is a rare congenital anomaly and is frequently associated with duplication of the urinary tract and rectosigmoid, and commonly associated with vertebral anomalies. Remzi reported less than 100 cases of duplication of all or a portion of the penis, but about 10 cases of complete diphallus with exstrophy of cloaca was reported, and a case of complete diphallus associated with hingut duplication was reported, and complete diphallus with displacement of bladder associated hindgut duplication and imperforate anus was not reported in Korea. We experienced a case of the complete diphallus associated with displacement of bladder, hindgut duplication, and imperforate anus as a variant of cloacal exstrophy. A review of published cases suggests that this may be the first example of a complete dip hall us with displacement of bladder coexisting with the hindgut duplication and imperforate anus.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Anus Imperfurado
/
Pênis
/
Sistema Urinário
/
Bexiga Urinária
/
Cloaca
/
Coreia (Geográfico)
País/Região como assunto:
Ásia
Idioma:
Coreano
Revista:
Journal of the Korean Association of Pediatric Surgeons
Ano de publicação:
1995
Tipo de documento:
Artigo
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