Login / Signup

Black liver in a patient with Wilson's disease.

Wei JiangQingmin ZengChang-Hai LiuDong-Bo WuHong Tang
Published in: Clinical case reports (2022)
Wilson's disease is an autosomal recessive inherited disease with congenital copper metabolism disorder, characterized by decreased ceruloplasmin and increased urine copper, which can involve multiple organs. This case was complicated by iron overload, which is of great value in differentiating hereditary hemochromatism.
Keyphrases
  • case report
  • computed tomography
  • contrast enhanced
  • iron deficiency