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Orthotopic Liver Transplantation in an Adult with Cholesterol Ester Storage Disease

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Part of the book series: JIMD Reports ((JIMD,volume 8))

Abstract

Cholesterol ester storage disease (CESD) is a rare autosomal recessive lipid storage disorder associated with mutations of the gene encoding lysosomal acid lipase, manifestations of which include chronic liver disease and early atherosclerosis. Although normally presenting in childhood, severity is variable and the condition can occasionally remain undetected until middle age. Typical presentation is with asymptomatic hepatosplenomegaly and hyperlipidaemia, though the condition is probably underdiagnosed. Treatment is supportive and may include attention to cardiovascular risk factors. Phase I/II trials of enzyme replacement therapy are ongoing, but this approach remains experimental. We present the case of a 42-year-old woman diagnosed with CESD in childhood who ran an indolent course until re-presentation with cirrhotic hydrothorax. She underwent orthotopic liver transplantation but required re-transplantation for hepatic artery thrombosis. She remains well with excellent graft function 2 years later. Although atherosclerosis was apparent at assessment, and may have contributed to hepatic artery thrombosis, partial correction of the metabolic defect and restoration of liver function by transplantation together with ongoing medical therapy should permit reasonable survival over the longer term from both a liver and a vascular perspective. This is the first reported case of orthotopic liver transplantation for CESD in an adult, which was the only available option to improve survival. The case highlights the importance of monitoring patients with CESD through adulthood and suggests that liver replacement at a later stage may yet be indicated and remain of benefit.

Competing interests: None declared

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Correspondence to Graeme K Ambler .

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Communicated by: Frits Wijburg

Appendices

Synopsis

Regular follow-up of liver function in adults with cholesterol ester storage disease, an uncommon lipid storage disorder, is an important consideration as orthotopic liver transplantation may be required to maintain long-term survival.

Conflicts of Interest and Financial Disclosures

The authors would like to thank Synageva Biopharma Corporation for providing the chromatograms in Fig. 3.

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© 2012 SSIEM and Springer-Verlag Berlin Heidelberg

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Ambler, G.K. et al. (2012). Orthotopic Liver Transplantation in an Adult with Cholesterol Ester Storage Disease. In: Zschocke, J., Gibson, K., Brown, G., Morava, E., Peters, V. (eds) JIMD Reports - Case and Research Reports, 2012/5. JIMD Reports, vol 8. Springer, Berlin, Heidelberg. https://doi.org/10.1007/8904_2012_155

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  • DOI: https://doi.org/10.1007/8904_2012_155

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  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-33432-0

  • Online ISBN: 978-3-642-33433-7

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