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Cholestatic liver disease in long-term infantile nephropathic cystinosis
Background: Cystinosis is a metabolic disease characterized by accumulation of cystine in different organs and tissues, leading to potentially life‐threatening organ dysfunction. Infantile cystinosis typically leads to end‐stage renal disease, necessitating renal replacement therapy. Liver disease...
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Published in: | Journal of gastroenterology and hepatology 2008-08, Vol.23 (8pt2), p.e428-e431 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Background: Cystinosis is a metabolic disease characterized by accumulation of cystine in different organs and tissues, leading to potentially life‐threatening organ dysfunction. Infantile cystinosis typically leads to end‐stage renal disease, necessitating renal replacement therapy. Liver disease in cystinosis is rare and is mostly reported as nodular regenerative hyperplasia leading to portal hypertension.
Methods: Two patients with infantile cystinosis developed cholestatic liver disease (increasing alkaline phosphatases, gamma‐glutamyltransferase and mild increase in transaminases). Severe accumulation of cystine was demonstrated on liver biopsy, predominantly localized in Kupffer cells, together with morphological signs of sclerosing cholangitis on liver biopsy. One patient showed changes compatible with sclerosing cholangitis on magnetic resonance imaging. Therapy with ursodeoxycholic acid led to biochemical improvement in one and stabilization in the other patient.
Conclusion: Long‐term infantile nephropathic cystinosis can be associated with a form of sclerosing cholangitis, which can respond to therapy with ursodeoxycholic acid. |
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ISSN: | 0815-9319 1440-1746 |
DOI: | 10.1111/j.1440-1746.2008.05312.x |