Literature DB >> 2035335

Neonatal Dubin-Johnson syndrome with severe cholestasis: effective phenobarbital therapy.

A Kimura1, K Ushijima, M Kage, R Mahara, M Tohma, T Inokuchi, K Shibao, N Tanaka, T Fujisawa, E Ono.   

Abstract

We described Dubin-Johnson syndrome (DJS) with severe cholestasis in a 20-day-old Japanese boy. Although neonatal DJS has been sporadically reported. DJS with severe cholestasis has not to our knowledge been described in the English literature. The ratio of urinary coproporphyrin isomer I to urinary total coproporphyrin in our patient was high (93%). Liver histology showed cytoplasmic pigment granules in the liver cells. Administration of phenobarbital (PB) significantly decreased the levels of bilirubin and bile acids in the serum. There was a significant elevation of 1 beta-hydroxylated bile acids in the urine. It is predicted that severe cholestasis in neonatal DJS may cause metabolic abnormalities in both bilirubin and bile acids transport.

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Year:  1991        PMID: 2035335     DOI: 10.1111/j.1651-2227.1991.tb11867.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  1 in total

1.  Ultrastructure of Kupffer cells and hepatocytes in the Dubin-Johnson syndrome: a case report.

Authors:  Maria Elzbieta Sobaniec-Lotowska; Dariusz Marek Lebensztejn
Journal:  World J Gastroenterol       Date:  2006-02-14       Impact factor: 5.742

  1 in total

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