Carolis disease: 6 case studies
Acta gastroenterol. latinoam
; 33(1): 47-51, 2003.
Article
in Es
|
LILACS-Express
| LILACS, BINACIS
| ID: biblio-1157308
Responsible library:
AR40.1
Localization: [{"text": "AR40.1"}]
ABSTRACT
Carolls disease is characterized by congenital non-obstructive dilatation of the intrahepatic bile ducts of undefined etiology. It is a rare disease usually affecting the whole liver but it may affect a lobe or a segment (11). This study shows the evolution of 6 cases (2 boys and 4 giris) that were diagnosed with Carolis disease at a referral service. Their ages ranged from 2 to 16 years--median age 10 years. One of the patients presented with cholangitis, while hepatomegaly was observed in 83
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Collection:
01-internacional
/
06-national
/
AR
Database:
BINACIS
/
LILACS
Language:
En
/
Es
Journal:
Acta gastroenterol. latinoam
Journal subject:
GASTROENTEROLOGIA
Year:
2003
Document type:
Article
Country of publication:
Argentina