End stage liver disease in a 13-year old secondary to hepatitis C and hemochromatosis

Mark Miller, Jeffrey S. Crippin, Göran Klintmalm

Research output: Contribution to journalArticle

5 Scopus citations

Abstract

Hepatic parenchymal iron deposition is a well known complication of chronic hepatic inflammatory states. This can make the differential between chronic hepatitis and hereditary hemochromatosis difficult, however. The case of a 13-yr-old male with chronic hepatitis C and hereditary hemochromatosis resulting in end stage liver disease and the need for orthotopic liver transplantation is described. There has been no previously described case of the coexistence of these two diseases in a pediatric patient, resulting in end stage liver disease. The progression to cirrhosis in a patient of this age suggests a more rapid progression of the combined diseases than with either disease alone.

Original languageEnglish
Pages (from-to)1427-1429
Number of pages3
JournalAmerican Journal of Gastroenterology
Volume91
Issue number7
StatePublished - Jul 1 1996
Externally publishedYes

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