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Hepatocellular carcinoma: Power Doppler US with a contrast agent - Preliminary results

Authors
Kim A.Y.Choi B.I.Kim T.K.Han J.K.Yun E.J.Lee K.Y.Han M.C.
Issue Date
1998
Publisher
Radiological Society of North America Inc.
Keywords
Contrast media; Galactose; Liver neoplasms, blood supply; Ultrasound (US), contrast media; Ultrasound (US), power Doppler studies
Citation
Radiology, v.209, no.1, pp 135 - 140
Pages
6
Indexed
SCOPUS
Journal Title
Radiology
Volume
209
Number
1
Start Page
135
End Page
140
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/25024
DOI
10.1148/radiology.209.1.9769824
ISSN
0033-8419
1527-1315
Abstract
PURPOSE: To investigate the value of contrast material-enhanced power Doppler ultrasonography (US) in the demonstration and characterization of tumor vascularity in hepatocellular carcinoma (HCC). MATERIALS AND METHODS: Twenty patients with HCC were prospectively evaluated with power Doppler US before and after injection of the contrast agent SH U 508 A. The grade and pattern of tumor vascularity at power Doppler US were analyzed, along with the degree of tumor staining at angiography. RESULTS: Intra- and peritumoral flow signals were detected in 19 HCCs (95%) at unenhanced power Doppler US. After injection of contrast agent, flow signals increased in 19 lesions (95%). At contrast-enhanced power Doppler US, two tumors demonstrated grade 1 vascularity; four grade 2; three, grade 3; and 11, grade 4. At angiography, two tumors demonstrated grade 1 staining; four grade 2; eight, grade 3; six, grade 4. The correlation between vascularity grades at contrast-enhanced power Doppler US and at angiography was statistically significant (P < .0001). Seventeen HCCs (85%) showed the intratumoral or basket pattern of vascularity at unenhanced power Doppler US; after injection of contrast material, 15 HCCs (75%) showed the mixed pattern. CONCLUSION: Contrast- enhanced power Doppler US is superior to unenhanced power Doppler US in the demonstration and characterization of tumor vascularity in HCC.
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