TY - JOUR
T1 - Recent developments in imaging diagnostics for HCC
T2 - CT arteriography and CT arterioportography evaluation of vascular changes in premalignant and malignant hepatic nodules
AU - Honda, Hiroshi
AU - Tajima, Tsuyoshi
AU - Taguchi, Kenichi
AU - Kuroiwa, Toshiro
AU - Yoshimitsu, Kengo
AU - Irie, Hiroyuki
AU - Aibe, Hitoshi
AU - Shinozaki, Kenji
AU - Asayama, Yoshiki
AU - Shimada, Mitsuo
AU - Masuda, Kouji
PY - 2000/1/1
Y1 - 2000/1/1
N2 - We analyzed the hemodynamic properties and vascular supply changes in relation to the carcinogencsis of hepatocellular carcinoma (HCC), selecting 18 premalignant and malignant nodules less than 3 cm diameter (from 14 patients) for our study. The computed tomographic (CT) arteriography and CT arterioportography (CTAP) findings for these nodules were correlated with the histopathologic findings. The ratios of all microscopically counted arteries (normal hepatic and abnormal arteries), normal hepatic arteries, and portal veins in each nodule to those in the surrounding liver were calculated. Well differentiated lesions had low attenuation on CT arteriography and isoattenuation on CTAP. Moderately-to-poorly differentiated lesions had high attenuation on CT arteriography and low attenuation on CTAP. In well differentiated lesions, the ratios of all arteries, normal hepatic arteries, and portal veins were 1.17 ± 0.10, 0.66 ± 0.12, and 0.80 ± 0.10, respectively. In moderately-to-poorly differentiated lesions, the ratios were 2.64 ± 0.23, 0.09 ± 0.03, and 0.07 ± 0.03, respectively. We concluded that blood flow does not parallel the actual number of arteries seen on the histological examination of tumors. In well differentiated lesions, the combination of normal hepatic arterial degeneration and preserved portal veins results in low attenuation on CT arteriography and isoattenuation on CTAP. In advanced HCC, the combination of neoplastic (abnormal) arterial development by angiogenesis and obliteration of portal veins results in high attenuation on CTA and low attenuation on CTAP. These findings are characteristic of early and advanced stage HCC, and may reflect a combination of sequential changes in their hemodynamic states.
AB - We analyzed the hemodynamic properties and vascular supply changes in relation to the carcinogencsis of hepatocellular carcinoma (HCC), selecting 18 premalignant and malignant nodules less than 3 cm diameter (from 14 patients) for our study. The computed tomographic (CT) arteriography and CT arterioportography (CTAP) findings for these nodules were correlated with the histopathologic findings. The ratios of all microscopically counted arteries (normal hepatic and abnormal arteries), normal hepatic arteries, and portal veins in each nodule to those in the surrounding liver were calculated. Well differentiated lesions had low attenuation on CT arteriography and isoattenuation on CTAP. Moderately-to-poorly differentiated lesions had high attenuation on CT arteriography and low attenuation on CTAP. In well differentiated lesions, the ratios of all arteries, normal hepatic arteries, and portal veins were 1.17 ± 0.10, 0.66 ± 0.12, and 0.80 ± 0.10, respectively. In moderately-to-poorly differentiated lesions, the ratios were 2.64 ± 0.23, 0.09 ± 0.03, and 0.07 ± 0.03, respectively. We concluded that blood flow does not parallel the actual number of arteries seen on the histological examination of tumors. In well differentiated lesions, the combination of normal hepatic arterial degeneration and preserved portal veins results in low attenuation on CT arteriography and isoattenuation on CTAP. In advanced HCC, the combination of neoplastic (abnormal) arterial development by angiogenesis and obliteration of portal veins results in high attenuation on CTA and low attenuation on CTAP. These findings are characteristic of early and advanced stage HCC, and may reflect a combination of sequential changes in their hemodynamic states.
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U2 - 10.1007/s005340070044
DO - 10.1007/s005340070044
M3 - Article
C2 - 10982622
AN - SCOPUS:0033649007
SN - 1868-6974
VL - 7
SP - 245
EP - 251
JO - Journal of Hepato-Biliary-Pancreatic Sciences
JF - Journal of Hepato-Biliary-Pancreatic Sciences
IS - 3
ER -