Patients who are treated for pediatric malignancy prior to donor screening for the hepatitis C virus (HCV) are at a high risk of acquiring HCV from the blood product transfusions that they receive [1]. Moreover, hepatitis C is symptomatic in 10% of cases; the acute illness is generally asymptomatic and 70-80% of patients develop chronic infection [1,2]. HCV could make the outcome of successfully treated pediatric oncology patients worse, because they receive a hepatotoxic drug during therapy [1, 3, 4]. It has recently been shown that antimetabolite chemotherapy exposure leads to a more rapid progression to fibrosis [1,5]. At present, the management of patients with hepatitis C focuses largely on combination antiviral treatment using a 24-or 48-week course of peg interferon and ribavirin [6, 7].Our clinics follow 408 patients who were treated for malignancy (leukemia and lymphoma) and blood product transfusions before 1990 when there were no tests available for detecting HCV in blood products. These patients have been screened for HBV and HCV. Patients were tested for antibody to HCV and HBV and for serum PCR-RNA and genotype at the follow-up.Seven children (5 males and 2 females) of 408 patients who were cured of a pediatric malignancy disease (median follow-up 11 years, range 7-15 years) entered the present study. All patients received at least 3 blood products (range 3-60) by transfusion with a median 14 ± 2.9 transfusions.All patients had chronic HCV infection defined by detectable circulating HCV-RNA. One patient had hepatitis B, C. Liver biopsies were performed.