2005
DOI: 10.1007/bf02734154
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Benign recurrent intrahepatic cholestasis

Abstract: Benign recurrent intrahepatic cholestasis (BRIC) is a rare cause of cholestasis in children. The disease may start in infancy or early childhood. Jaundice persists or recurs throughout life but does not lead to chronic liver disease or cirrhosis. Treatment is mostly symptomatic. The condition has not been reported in Indian children. We report an interesting case of BRIC in a 9-year-old boy who had recurrent episodes of jaundice since when he was 1 yr old.

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Cited by 11 publications
(7 citation statements)
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“…Approximately 100 cases of BRIC have been reported till date. [11,12,13] In a case of a 47 year old female with psoriasis with history of methotrexate intake with a high cumulative dose since 2 years. Liver biopsy was done which showed hepatocytes with mild ballooning degeneration, mild macrovesicular steatosis and mild periportal fibrosis.…”
Section: Discussionmentioning
confidence: 99%
“…Approximately 100 cases of BRIC have been reported till date. [11,12,13] In a case of a 47 year old female with psoriasis with history of methotrexate intake with a high cumulative dose since 2 years. Liver biopsy was done which showed hepatocytes with mild ballooning degeneration, mild macrovesicular steatosis and mild periportal fibrosis.…”
Section: Discussionmentioning
confidence: 99%
“…The transaminases are usually in normal range but can increase up to 200-400 U/L [4]. The disease follows a benign course and there is no progression to cirrhosis [5]. However, a case report has revealed that some patients initially presenting with clinical features of BRIC may later progress to progressive familial intrahepatic cholestasis.…”
Section: Discussionmentioning
confidence: 99%
“…These signs may persist or recur throughout life but do not lead to chronic liver disease or cirrhosis [2,3]. The treatment of BRIC is purely symptomatic.…”
Section: Discussionmentioning
confidence: 99%
“…The treatment of BRIC is purely symptomatic. There are conflicting reports regarding the effect of therapeutic alternatives such as UDCA, cholestyramin and rifampicin [3][4][5]. CTS is also rare in childhood.…”
Section: Discussionmentioning
confidence: 99%