A 68-year old mildly obese Caucasian man underwent hepatic resection for mu
ltinodular hepatocellular carcinoma which had developed in the left lobe of
non-cirrhotic liver. The only risk factors found were heavy drinking, smok
ing, and serum markers of hepatitis B virus without virus genome in hepatoc
ytes. The non tumoral liver was mildly fibrotic and iron overloaded (hepati
c iron index: 1.6) with three types of iron-free lesions: (i) periportal cl
ear hepatocyte foci, (ii) hyperplastic nodules and (iii) dysplastic or neop
lastic nodules with well to moderately-differentiated hepatocellular carcin
oma. The genetic investigation was negative for the C282Y and the H63D muta
tions of the HFE gene. This observation illustrates the multistep process o
f carcinogenesis in the non-cirrhotic liver and raises the question of i) t
he origin of this iron overload possibly linked to insulin resistance syndr
ome and ii) the role of iron as a co-carcinogen.