A Case of Nonfamilial Benign Recurrent Intrahepatic Cholestasis / 대한간학회지
The Korean Journal of Hepatology
;
: 188-193, 1998.
Artigo
em Coreano
| WPRIM
| ID: wpr-144294
ABSTRACT
Benign recurrent intrahepatic cholestasis (BRIC) is a rare desease, which usually manifests between the age of 10 and 20. Its main clinical feature is multiple recurrent episodes of cholestasis without extrahepatic bile duct obstruction. We report here a case of nonfamilial benign recurrent intrahepatic cholestasis. The patient has experienced recurrent jaundice with pruritus since childhood. Main bile duct obstrution was excluded by abdominal CT and endoscopic retrograde cholangiopancreatography. Other causes of cholestasis were not found. Hepatic histology revealed bile plug which were mainly concentrated in the centrilobular region, and increased number of mononuclear cells in the portal triad, but hepatic parenchyma showed no inflammation and necrosis. In the last anicteric period, she was healthy and the liver function test and biopsy specimen were normal.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Prurido
/
Bile
/
Ductos Biliares
/
Biópsia
/
Tomografia Computadorizada por Raios X
/
Colestase
/
Colestase Intra-Hepática
/
Colangiopancreatografia Retrógrada Endoscópica
/
Ductos Biliares Extra-Hepáticos
/
Inflamação
Limite:
Humanos
Idioma:
Coreano
Revista:
The Korean Journal of Hepatology
Ano de publicação:
1998
Tipo de documento:
Artigo
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