Hepatocellular carcinoma in the thalassaemia syndromes

Summary 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 t...

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Veröffentlicht in:British journal of haematology 2004-01, Vol.124 (1), p.114-117
Hauptverfasser: Borgna‐Pignatti, Caterina, Vergine, Gianluca, Lombardo, Turi, Cappellini, Maria Domenica, Cianciulli, Paolo, Maggio, Aurelio, Renda, Disma, Lai, Maria Eliana, Mandas, Antonella, Forni, Gianluca, Piga, Antonio, Bisconte, Maria Grazia
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Sprache:eng
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Zusammenfassung:Summary 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 μg/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.
ISSN:0007-1048
1365-2141
DOI:10.1046/j.1365-2141.2003.04732.x