Twenty-three cases of HCC were selected for transcatheter arterial chemoembolization therapy in our institution between January 2000 and March 2001. The size of the lesions ranged between 18 and 56 mm in diameter (mean size, 32 mm). Nineteen cases were men and 4 were women (mean age, 58 years). All patients had cirrhosis of the liver, 16 patients had posthepatic cirrhosis and 7 had alcoholic cirrhosis. Hepatocellular carcinomas were diagnosed by means of sonographically guided percutaneous biopsy. The hepatic lesions were examined with contrast-enhanced PDU before and one and six months after the interventional procedure. Of the 23 tumors, twelve lesions were also studied with contrast-enhanced wideband harmonic imaging (WHI). In our study we used a Sonoline Elegra ultrasound system (Siemens Medical Systems, Issaquah, WA) with wideband harmonic imaging (EnsembleTM Contrast Imaging) installed on a 3,5 MHz convex transducer (3.5C40 transducer). The sonographic examination began with a real-time B-mode study of the liver in order to localize the lesions and select the best scan plane. Then, an unenhanced power Doppler exam of the lesion was performed with low-pulse repetition frequency for detection of tiny vascular structures. This examination was repeated after intravenous administration of 2,5 gr. of a galactose-based ultrasound contrast agent (Levovist®, Schering AG, Berlin, Germany) at a concentration of 300 mg/ml, and presence of arterial flow inside and/or at the periphery of the lesion was evaluated. Spectrum analysis of these vessels was obtained, if possible. In 12 cases we also performed a contrast-enhanced wideband harmonic exam of the lesions. Wideband harmonic imaging was performed by the same radiologist, with previous setting of the following parameters: frequency of 2–2,5 MHz, single focal zone, parallel processing on, maximum frame rate ( 10/sec), persistence off and medium line density (RES/SPEED 3 or 4). A second injection of contrast agent at the same concentration was administered and the liver was scanned intermittently during the first 60 seconds, and 3 minutes after the injection in order to study the liver specific phase of Levovist. Images were obtained 20, 40 and 60 seconds after administration of contrast agent and 3 minutes later in order to evaluate the arterial, capillary and late phase of enhancement of the tumours. The images were stored digitally on the hard disk in the US scanner. The examinations were also recorded on videotape. The outcome of therapy was established by means of unenhanced and enhanced spiral CT exam. Spiral CT was performed with a Toshiba Asteion TSX-021A equipment Acad Radiol 2002; 9(suppl 2):S382–S383
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