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Hepatocellular carcinoma
Diagnosis

Updated: October 29, 2005

Imaging

Ultrasound

The initial diagnostic test in the symptomatic patient may be ultrasonography, as it is noninvasive and can detect lesions as small as 1 cm. Ultrasound findings should be followed up with more specific imaging. Ultrasound guided biopsies may be used to establish the diagnosis.

CT and MRI

Triple-phase, high-resolution CT and contrast-enhanced MRI are the primary imaging modalities used to diagnose and stage hepatocellular carcinoma. CT scan predicts resectability in only 40%-50% of cases and does not accurately determine the functional extent of cirrhosis. Major difficulties arise when the liver parenchyma is not homogeneous and the lesions are smaller than 1 cm.

Grossly, metastatic tumors are often peripheral and multiple and cause umbilication of the surface of the liver, whereas primary liver tumors are more often central and can be solitary, but are usually hypervascular on the arterial phase of a helical CT scan.

Invasion of the portal vein and to a lesser extent the hepatic vein is typically seen on dynamic CT as an obstruction of portal flow with venous expansion, which thus distinguishes malignant from benign thrombosis. Malignant thrombi are often hypervascular on the arterial phase of the CT, whereas bland thrombi are not hypervascular.

Biopsy

Some authors believe that percutaneous liver biopsy carries a high risk and has little diagnostic value. Nevertheless, a biopsy is imperative to establish the diagnosis either by percutaneous technique or by surgery.

Laparoscopy

Laparoscopy is useful for the evaluation of small tumors, the extent of cirrhosis, peritoneal seeding, and the volume of noninvolved liver and therefore may be used prior to open laparotomy for resection. Laparoscopic or intraoperative ultrasonography should be used to confirm preoperative imaging tests. The laparoscopic results may change surgical management in up to one third of selected patients.

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Labs

α-Fetoprotein is produced by 70% of hepatocellular carcinomas. The normal range for this serum marker is 0-20 ng/mL, and a level > 200 ng/mL is essentially diagnostic for hepatocellular cancer in the absence of chronic, active hepatitis B infection. In the presence of active hepatitis B infection, the diagnostic cutoff is considered to be at least 1,000 ng/mL. In the setting of hepatitis  C infection, the cutoff for diagnosis of hepatocellular carcinoma has not been well studied. False-positive results may be due to acute or chronic hepatitis, germ-cell tumors, or pregnancy.

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