A Case of Congenital Agenesis of the Gallbladder without Biliary Atresia associated with Duodenal Web
Journal of the Korean Society of Neonatology
;
: 117-122, 2005.
Artículo
en Coreano
| WPRIM
| ID: wpr-94002
ABSTRACT
Congenital absence of the gall bladder without extrahepatic biliary atresia is an extremely rare congenital malformation with a reported incidence ranging between 0.01 and 0.02%. It is thought to be occurred from failure of the gallbladder bud to develop in utero and frequent association with other malformations. Agenesis can be randomly discovered at autopsy or operations for symptoms suggestive of biliary tract disease. The authors report a case of agenesis of the gallbladder without extrahepatic biliary atresia in a neonate which was incidentally found at laparotomy for presumed duodenal obstruction, with a review of the literature.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Autopsia
/
Enfermedades de las Vías Biliares
/
Vejiga Urinaria
/
Atresia Biliar
/
Incidencia
/
Obstrucción Duodenal
/
Vesícula Biliar
/
Laparotomía
Tipo de estudio:
Estudio de incidencia
/
Estudio pronóstico
Límite:
Humanos
/
Recién Nacido
Idioma:
Coreano
Revista:
Journal of the Korean Society of Neonatology
Año:
2005
Tipo del documento:
Artículo
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