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Abstract Summary and conclusion Hepatocellular carcinoma (HCC) is one of the most common malignant tumors worldwide. In Egypt, the incidence of HCC has doubled in the past 10 years and it is now the second most incident and lethal cancer. Early detection is critically important because the effective treatment for HCC is surgical resection or ablation therapy when the tumor is small. Up to 20% of HCC cases do not produce AFP, even when very large, and slight increases are usual in acute hepatitis, chronic hepatitis and cirrhosis and overlaps can cause diagnostic difficulties. Thus, the identification of novel biochemical markers for HCC remains an important goal for many laboratories around the world. One of these biomarkers is “Fucosylated Haptoglobin”. Our study was performed to evaluate fucosylated haptoglobin as a biomarker for hepatocellular carcinoma in Egyptian patients. This prospective study was carried out on 60 patients classified into three groups; group (I): 20 patients with HCC, group (II): 20 patients with cirrhotic liver disease without HCC and group (III) (the control group): 20 apparently healthy individuals. Inclusion criteria were adult patient, diagnosis of liver cirrhosis (based on clinical, biochemical and radiological criteria “by US (coarse echogenic pattern, bulky caudate lobe, attenuated hepatic veins” with or without liver biopsy)) and diagnosis of HCC was by the following criteria: Pathological HCC diagnosis by percutaneous biopsy, or Clinical and radiological (by ultrasound and triphasic CT). Exclusion criteria were: patient refusal, diabetes mellitus, chronic renal impairment, patients with extrahepatic metastases, other neoplasm, previous history of HCC ablation and pathological or radiological evidence of mixed HCC-cholangio cellular carcinoma. |