Hepatic entropy and uniformity: additional parameters that can potentially increase the effectiveness of contrast enhancement during abdominal CT

被引:68
作者
Ganeshan, B. [1 ]
Miles, K. A.
Young, R. C. D.
Chatwin, C. R.
机构
[1] Univ Sussex, Dept Engn & Design, Brighton BN1 9QT, E Sussex, England
[2] Brighton & Sussex Med Sch, Div Clin & Lab Sci, Brighton, E Sussex, England
关键词
D O I
10.1016/j.crad.2007.03.004
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
AIM: To determine how hepatic entropy and uniformity of computed tomography (CT) images of the liver change after the administration of contrast material and to assess whether these additional parameters are more sensitive to tumour-related changes in the liver than measurements of hepatic attenuation or perfusion. MATERIALS AND METHODS: Hepatic attenuation, entropy, uniformity, and perfusion were measured using multiphase CT following resection of colorectal cancer. Based on conventional CT and fluorodeoxyglucose positron emission tomography, 12 patients were classified as having no evidence of malignancy, eight with extra-hepatic tumours; only, and eight with metastatic liver disease. RESULTS: Hepatic attenuation and entropy increased after CM administration whereas uniformity decreased. Unlike hepatic attenuation, entropy and uniformity changed maximally in the arterial phase. No significant differences in hepatic perfusion or attenuation were found between patient groups, whereas arterial-phase entropy was tower (p = 0.034) and arterial-phase uniformity was higher (p = 0.034) in apparently disease-free areas of liver in patients with hepatic metastases compared with those with no metastases. CONCLUSION: Temporal changes in hepatic entropy and uniformity differ from those for hepatic attenuation. By reflecting the distribution of hepatic enhancement, these additional parameters are more sensitive to tumour-retated changes in the liver than measurements of hepatic attenuation or perfusion. (c) 2007 The Royal College of Radiologists. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:761 / 768
页数:8
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