PT - JOURNAL ARTICLE AU - R Moucari AU - P-E Rautou AU - D Cazals-Hatem AU - A Geara AU - C Bureau AU - Y Consigny AU - C Francoz AU - M-H Denninger AU - V Vilgrain AU - J Belghiti AU - F Durand AU - D Valla AU - A Plessier TI - Hepatocellular carcinoma in Budd–Chiari syndrome: characteristics and risk factors AID - 10.1136/gut.2007.139477 DP - 2008 Jun 01 TA - Gut PG - 828--835 VI - 57 IP - 6 4099 - http://gut.bmj.com/content/57/6/828.short 4100 - http://gut.bmj.com/content/57/6/828.full SO - Gut2008 Jun 01; 57 AB - Background and aim: To analyse the characteristics of and the factors associated with the development of hepatocellular carcinoma (HCC) in patients with Budd–Chiari syndrome (BCS). Patients and methods: 97 consecutive patients with BCS and a follow-up ⩾1 year were evaluated retrospectively. Liver nodules were evaluated using serum α-fetoprotein (AFP) level and imaging features (CT/MRI). Biopsy of nodules was obtained when one of the following criteria was met: number ⩽3, diameter ⩾3 cm, heterogeneity, washout on portal venous phase, increase in size on surveillance, or increase in AFP level. Results: Patients were mainly Caucasian (69%) and female (66%). Mean age at the diagnosis of BCS was 35.8 (SE 1.2 years), and median follow-up 5 years (1–20 years). The inferior vena cava (IVC) was obstructed in 13 patients. Liver nodules were found in 43 patients, 11 of whom had HCC. Cumulative incidence of HCC during follow-up was 4%. Liver parenchyma adjacent to HCC showed cirrhosis in nine patients. HCC was associated with male sex (72.7% v 29.0%, p = 0.007); factor V Leiden (54.5% v 17.5%, p = 0.01); and IVC obstruction (81.8% v 4.6%, p<0.001). Increased levels of serum AFP were highly accurate in distinguishing HCC from benign nodules: PPV = 100% and NPV = 91% for a cut-off level of 15 ng/ml. Conclusion: The incidence of HCC in this large cohort of BCS patients was similar to that reported for other chronic liver diseases. IVC obstruction was a major predictor for HCC development. Serum AFP appears to have a higher utility for HCC screening in patients with BCS than with other liver diseases.