Hepatocellular carcinoma in the thalassaemia syndromes

Br J Haematol. 2004 Jan;124(1):114-7. doi: 10.1046/j.1365-2141.2003.04732.x.

Abstract

Hepatocellular carcinoma (HCC) frequently complicates hepatic cirrhosis secondary to viral infection or iron overload. Therefore, patients affected by thalassaemia syndromes have a theoretically high risk of developing the tumour. We collected data on patients attending Italian centres for the treatment of thalassaemia. Twenty-two cases of HCC were identified; 15 were male. At diagnosis, the mean age was 45 +/- 11 years and the mean serum ferritin was 1764 +/- 1448 microg/l. Eighty-six percent had been infected by hepatitis C virus. Nineteen of 22 cases were diagnosed after 1993, suggesting that this problem is becoming more frequent with the aging population of thalassaemia patients.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Carcinoma, Hepatocellular / etiology*
  • Female
  • Hepatitis C / complications
  • Humans
  • Iron Overload / complications
  • Liver Cirrhosis / etiology
  • Liver Neoplasms / etiology*
  • Male
  • Middle Aged
  • Thalassemia / complications*
  • Thalassemia / therapy