A Case of Biliary Atresia with Ileal Atresia / 소아과
Korean Journal of Pediatrics
;
: 908-911, 2004.
Artigo
em Coreano
| WPRIM
| ID: wpr-148786
ABSTRACT
Biliary atresia is a progressive obliterative cholangiopathy. However, the actual causes remain unknown, although a number of factors such as developmental malformation, viral infection, toxicity of bile constituents, and anatomic abnormality in the hepatobiliary system have been considered. Recently, several studies have been done to find out specific gene expression. Some cases of biliary atresia are associated with anomalies of cardiovascular system, digestive tract and spleen. Few cases of biliary atresia with congenital ileal atresia were reported. We experienced a case with biliary atresia combined with ileal atresia. Ileal resection and end to end anastomosis operation were done at second days of the life because of congenital ileal atresia. Jaundice and acholic stool were noticed a few days after the operation. He was diagnosed as biliary atresia and received Kasai operation at 23 days of the life. Therefore, we report the case with a brief review of the related literature.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Baço
/
Bile
/
Atresia Biliar
/
Sistema Cardiovascular
/
Expressão Gênica
/
Trato Gastrointestinal
/
Icterícia
Idioma:
Coreano
Revista:
Korean Journal of Pediatrics
Ano de publicação:
2004
Tipo de documento:
Artigo
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