Management of Acute Wilsonian Hepatitis with Severe Hemolysis: A Successful Combination of Chelation and MARS Dialysis.
Jeremy HassounNathalie HammerGiulia MaginiBelén PonteMarie OngaroAnne-Laure RougemontNicolas GoossensJean-Louis FrossardLaurent SpahrPublished in: Case reports in hepatology (2021)
Wilson's disease is a rare hereditary disorder of copper metabolism leading to progressive accumulation of copper in several organs including the brain and the liver. Acute liver failure is a relatively rare hepatic manifestation of WD which may require urgent liver transplantation if medical treatment fails. We report here the case of a young woman who presented with classic acute Wilsonian hepatitis complicated by liver and renal failure and a severe hemolysis related to massive nonceruloplasmin bound copper accumulation requiring repeated blood transfusions. The early initiation of a combined treatment including conventional chelation therapy and repeated MARS dialysis sessions allowed a rapid control of hemolysis, a progressive decrease of free copper overload, and clinical recompensation without liver transplantation.
Keyphrases
- liver failure
- hepatitis b virus
- drug induced
- multiple sclerosis
- respiratory failure
- oxide nanoparticles
- early onset
- healthcare
- aortic dissection
- red blood cell
- stem cells
- white matter
- end stage renal disease
- intensive care unit
- cerebral ischemia
- extracorporeal membrane oxygenation
- brain injury
- middle aged
- blood brain barrier
- cell therapy