Atypical enhancement pattern of hepatocellular carcinoma with portal vein thrombosis on multiphasic CT

The 2005 American Association for Study of Liver Diseases (AASLD) diagnostic criteria allow non-invasive diagnosis of hepatocellular carcinoma (HCC) based on their enhancement pattern but we have observed a high incidence of atypical enhancement characteristics in HCC associated with portal vein thr...

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Veröffentlicht in:Annals of the Academy of Medicine, Singapore Singapore, 2011-10, Vol.40 (10), p.454-459
Hauptverfasser: Thian, Yee Liang, Low, Albert S C, Chow, Pierce K H, Ooi, London L, Chung, Alexander Y F, Low, Shoen C S, Xie, Wanying, Thng, Choon Hua
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Sprache:eng
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Zusammenfassung:The 2005 American Association for Study of Liver Diseases (AASLD) diagnostic criteria allow non-invasive diagnosis of hepatocellular carcinoma (HCC) based on their enhancement pattern but we have observed a high incidence of atypical enhancement characteristics in HCC associated with portal vein thrombosis. This study seeks to examine the radiological features of this particular subgroup. Patients with HCC and portal vein thrombosis who underwent pre-treatment multiphasic CT imaging were drawn from a surgical database. The arterial, portal venous and delayed phase images were assessed qualitatively and quantitatively (with region of interest [ROI] analysis) for lesion hypervascularity and washout. The background enhancement of the left and right lobes of the liver was also quantifi ed by ROI analysis. Twenty-fi ve lesions in 25 patients were selected for analysis. Qualitative analysis showed that 10/25 (40%) lesions demonstrated arterial hypervascularity while 16/25 (64%) lesions showed washout. Ten out of 25 (40%) lesions demonstrated both arterial hypervascularity and washout. Quantitative analysis showed that the average absolute lesion enhancement from precontrast to arterial phases was 49.1 (± 17.1) HU for hypervascular lesions compared to 23.8 (± 16.6) HU for non-hypervascular lesions (P
ISSN:0304-4602
0304-4602
DOI:10.47102/annals-acadmedsg.V40N10p454