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Hepatocellular carcinoma: evaluation with biphasic, contrast-enhanced, helical CT

R L Baron1, J H Oliver, G D Dodd

  • 1Department of Radiology, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.

Radiology
|May 1, 1996
PubMed

Insights

Adding hepatic arterial-dominant phase (HAP) imaging to portal venous-dominant phase (PVP) computed tomography (CT) enhances hepatocellular carcinoma (HCC) detection. This biphasic approach optimizes HCC evaluation in at-risk patients.

Area of Science:

  • Radiology
  • Oncology
  • Medical Imaging

Background:

  • Hepatocellular carcinoma (HCC) is a primary liver malignancy.
  • Accurate detection and staging of HCC are crucial for effective patient management.
  • Contrast-enhanced computed tomography (CT) is a key imaging modality for HCC evaluation.

Purpose of the Study:

  • To assess the incremental value of hepatic arterial-dominant phase (HAP) imaging when combined with portal venous-dominant phase (PVP) imaging.
  • To determine if HAP imaging improves the detection of hepatocellular carcinoma (HCC) foci compared to PVP imaging alone.
  • To evaluate the utility of biphasic contrast-enhanced CT in HCC assessment.

Main Methods:

  • Sixty-six patients with confirmed HCC underwent biphasic contrast-enhanced CT.
  • Hepatic arterial-dominant phase (HAP) images were acquired between 20-50 seconds post-contrast.
  • Portal venous-dominant phase (PVP) images were acquired between 60-100 seconds post-contrast.

Main Results:

  • A total of 326 tumor foci were identified.
  • HAP imaging visualized 95% (309/326) of foci, while PVP imaging visualized 82% (268/326).
  • In 11% (7/66) of patients, HCC was detected exclusively on HAP images.
  • HAP imaging also improved the detection of malignant portal vein thrombosis.

Conclusions:

  • Combining HAP and PVP contrast-enhanced CT optimizes the detection and evaluation of HCC.
  • Biphasic CT imaging provides a more comprehensive assessment of HCC burden.
  • This approach is recommended for patients with or at risk for hepatocellular carcinoma.
Abstract

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