Hepatocellular carcinoma is an epithelial tumor derived from hepatocytes that accounts for more than 80% of all primary hepatic tumors. The severity of the underlying disease is almost always the key factor in deciding whether to consider liver resection or transplantation as its treatment. Data in our registry corresponding to almost 800 patients from transplant centers throughout the world showed that patient survival after liver transplantation was significantly affected by histologic grade, tumor size >5 cm, and the presence of positive nodes. Recurrencefree survival showed a correlation with tumor size >5 cm, positive nodes, bilobar spread, and vascular invasion. At the present time, 59% of patients in our registry are alive, 84% of whom are free of tumor. Of those who died, half did so without evidence of tumor. (Liver Transpl 2002;8: 736-748.) P rimary hepatic tumors can be epithelial, mesenchymal, or mixed in nature. Hepatocellular carcinoma (HCC), an epithelial tumor derived from hepatocytes, accounts for more than 80% of all such malignancies. It affects men three times more frequently than women and is almost always associated with underlying hepatic cirrhosis. 1,2 There is a strong association between hepatitis B (HBV) and HCC, especially in non-Western countries. [3][4][5][6] In Western countries, cirrhosis associated with alcoholism and hepatitis C (HCV) infection shows the strongest association. 1,7 When associated with cirrhosis, HCC usually presents as a nodular, encapsulated, and well-circumscribed tumor. In advanced stages it becomes infiltrative or expansile with associated satellite lesions within the liver parenchyma. The right lobe of the liver tends to be involved more frequently than the left lobe. Multifocal tumors may or may not represent independent entities. Bilobar masses are not infrequent. Advanced cases show involvement of the portal vein sometimes manifest by a tumor thrombus. Hematogenous spread is more common than lymphatic dissemination. 1,8,9 Tumor cells may show a wide range of differentiation. 10,11 Ultrasound examination and serum alpha-fetoprotein levels are useful screening tools. Computerized tomography (CT) scanning has a detection rate for HCC lower than 70%. When combined with arteriography, sensitivity increases. Magnetic resonance imaging (MRI), especially in association with dynamic bolus gadolinium contrast, shows the highest detection rate. 1 Percutaneous fine needle biopsy (2% to 3% incidence of needle tract seeding) allows for histologic confirmation in cases of tumors with inconclusive characteristics. [12][13][14][15][16][17][18] At the time of diagnosis, 20% to 60% of small HCCs were found to be multifocal [19][20][21] and up to 30% of tumors in cirrhotic patients were understaged despite elaborate preoperative workups. 22
Materials and MethodsWe recently updated our worldwide registry, which now includes 973 patients, 790 of whom had a diagnosis of HCC. Three percent of these 790 patients had the fibrolamellar type of HCC. Seventy-three percent were male....