Liver Cancer
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Oct 15, 2003; 9(10): 2198-2201
Published online Oct 15, 2003. doi: 10.3748/wjg.v9.i10.2198
Role of multiphase scans by multirow-detector helical CT in detecting small hepatocellular carcinoma
Hong Zhao, Kang-Rong Zhou, Fu-Hua Yan
Hong Zhao, Department of Radiology, First Hospital, Shanxi Medical College, Taiyuan 030001, Shanxi Province, China
Kang-Rong Zhou, Fu-Hua Yan, Department of Radiology, Zhongshang Hospital, Fudan University, Shanghai 200032, China
Author contributions: All authors contributed equally to the work.
Supported by the Ministry Public Health Programme, No.97030220
Correspondence to: Dr. Hong Zhao, Department of Radiology, First Hospital, Shanxi Medical College, Taiyuan 030001, Shanxi Province, China. zhaohongmd@sina.com
Telephone: +86-351-4044111 Ext 24781
Received: March 12, 2003
Revised: April 7, 2003
Accepted: April 14, 2003
Published online: October 15, 2003
Abstract

AIM: To evaluate the role of multiphasic scanning by multirow-detector helical CT (MDCT) in detecing small hypervascular hepatocellular carcinoma (SHCC).

METHODS: Multiphasic scanning was carried out in 75 patients with SHCC with Marconi MX8000 CT scanner. The early arterial phase (EAP), late arterial phase (LAP) and the portal venous phase (PVP) scans were started at 21 s, 34 s and 85 s respectively. The mean difference of CT values between tumor and liver parenchyma for each scanning phase was measured, and the sensitivity of detection of SHCC in each of these phases and in the combined phase was calculated and statistically analyzed.

RESULTS: The mean difference of CT values between tumor and liver parenchyma was significant in 71 lesions ≥ 1 cm in three phases (P < 0.05). In 91 tumor foci, the detectability of SHCC was 45.1%, 83.5% and 92.3% in EAP, LAP and double arterial phases (DAP), respectively. The early arterial phase plus the portal venous phase and the double arterial phase plus the portal venous phase were 94.5%, 97.8%, respectively. Whereas the detectability in LAP plus PVP and in DAP plus PVP had no statistical difference.

CONCLUSION: The utility of faster speed and thinner slice MDCT and multiphase scanning protocol can improve the detectability of hypervascular small hepatocellular carcinoma. Among which LAP is superior to EAP in depicting the lesions.

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