Hepatocellular carcinoma risk assessment using gadoxetic acid‐enhanced hepatocyte phase magnetic resonance imaging

Nobutoshi Komatsu(University of Yamanashi), Utaroh Motosugi(University of Yamanashi), Shinya Maekawa(University of Yamanashi), Kuniaki Shindo(University of Yamanashi), Minoru Sakamoto(University of Yamanashi), Mitsuaki Sato(University of Yamanashi), Akihisa Tatsumi(University of Yamanashi), Mika Miura(University of Yamanashi), Fumitake Amemiya(University of Yamanashi), Yasuhiro Nakayama(University of Yamanashi), Taisuke Inoue(University of Yamanashi), Mitsuharu Fukasawa(University of Yamanashi), Tomoyoshi Uetake(University of Yamanashi), Masahiko Ohtaka(University of Yamanashi), Tadashi Sato(University of Yamanashi), Yasuhiro Asahina(Tokyo Medical and Dental University), Masayuki Kurosaki(Musashino Red Cross Hospital), Namiki Izumi(Musashino Red Cross Hospital), Tomoaki Ichikawa(University of Yamanashi), Tsutomu Araki(University of Yamanashi), Nobuyuki Enomoto(University of Yamanashi)
Hepatology Research
February 17, 2014
Cited by 45

Abstract

AIM: To investigate whether the patients with hypovascular liver nodules determined on the arterial phase and hypointensity on the hepatocyte phase gadoxetic acid-enhanced magnetic resonance imaging (hypovascular hypointense nodules) are at increased risk of hepatocarcinogenesis, we assessed subsequent typical hepatocellular carcinoma (HCC) development at any sites of the liver with and without such nodules. METHODS: One hundred and twenty-seven patients with chronic hepatitis B or C and without a history of HCC, including 68 with liver cirrhosis, were divided into those with (non-clean liver group, n = 18) and without (clean liver group, n = 109) hypovascular hypointense nodules. All the patients were followed up for 3 years, and HCC development rates and risk factors were analyzed with the Kaplan-Meier method and the Cox proportional hazard model, respectively. RESULTS: A total of 17 patients (10 in the non-clean liver group and seven in the clean liver group) developed typical HCC. Cumulative 3-year rates of HCC development were 55.5% in the non-clean liver group and 6.4% in the clean liver group (P < 0.001), and those at the different sites from the initial nodules was also higher in the non-clean liver group (22.2%) than the clean liver group (6.4%) (P = 0.003). Multivariate analysis identified older age (P = 0.024), low platelet counts (P = 0.017) and a non-clean liver (P < 0.001) as independent risk factors for subsequent HCC development. CONCLUSION: Patients with hypovascular hypointense liver nodules are at a higher risk for HCC development at any sites of the liver than those without such nodules.


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