Assessment of the severity of liver disease and fibrotic change: The usefulness of hepatic CT perfusion imaging

被引:76
作者
Hashimoto, Kazuhiko
Murakami, Takamichi
Dono, Keizo
Hori, Masatoshi
Kim, Tonsok
Kudo, Masayuki
Marubashi, Shigeru
Miyamoto, Atsushi
Takeda, Yutaka
Nagano, Hiroaki
Umeshita, Koji
Nakamura, Hironobu
Monden, Morito
机构
[1] Osaka Univ, Grad Sch Med, Dept Surg, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Med, Dept Radiol, Suita, Osaka 5650871, Japan
[3] GE Healthcare, Imaging Applicat Tech Ctr, Tokyo, Japan
关键词
hepatic tissue blood flow; CT perfusion; tissue blood volume; tissue blood flow; mean transit time; hepatic arterial fraction; liver fibrosis;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
This study assessed the utility of CT perfusion for quantitative assessment of liver function and fibrosis. Tissue blood flow (TBF), tissue blood volume (TBV), mean transit time (MTT) and hepatic arterial fraction (HAF) were measured with CT perfusion using the deconvolution algorithm in 38 patients with chronic liver diseases and 10 patients without liver disease. Using Child-Pugh classification, 21 patients were classified as Child A, 10 as Child B, and 7 as Child C. In 20 patients, the degree of fibrosis was quantitated in surgically-resected specimens and compared with the perfusion parameters. The mean TBF, TBV, MTT and HAF of patients without liver disease were 103.9 +/- 18 ml/min/100 g, 12.5 +/- 2.0 ml/100 g, 11.1 +/- 1.6 sec and 18.4 +/- 5.6%, respectively (+/- SD). The mean TBF of patients with Child A, B and C were 95.1 +/- 24, 86.7 +/- 29 and 75.5 +/- 6.5 ml/min/100 g, respectively. TBF tended to decrease with the severity of chronic liver disease. The mean HAF of patients with Child A, B and C were 18.6 +/- 8.3, 29.8 +/- 11.2 and 40.2 +/- 11.1%, respectively. HAF of patients without liver disease was significantly different from those of Child B and C (p < 0.05, each). However, there were no significant differences in TBV and MTT between each groups. HAF correlated significantly with the degree of fibrosis (R-2-0.588, p < 0.05). Our results showed that parameters of CT perfusion correlated significantly with the severity of liver fibrosis and cirrhosis. Quantitative measurement of hepatic tissue blood flow by CT perfusion is useful for evaluation of the severity of disease and fibrotic change.
引用
收藏
页码:677 / 683
页数:7
相关论文
共 47 条
[1]
Measurement of hepatic perfusion with dynamic computed tomography -: Assessment of normal values and comparison of two methods to compensate for motion artifacts [J].
Bader, TR ;
Grabenwöger, F ;
Prokesch, RW ;
Krause, W .
INVESTIGATIVE RADIOLOGY, 2000, 35 (09) :539-547
[2]
Hepatic perfusion after liver transplantation:: Noninvasive measurement with dynamic single-section CT [J].
Bader, TR ;
Herneth, AM ;
Blaicher, W ;
Steininger, R ;
Mühlbacher, F ;
Lechner, G ;
Grabenwöger, F .
RADIOLOGY, 1998, 209 (01) :129-134
[3]
LIVER PERFUSION STUDIED WITH ULTRAFAST CT [J].
BLOMLEY, MJK ;
COULDEN, R ;
DAWSON, P ;
KORMANO, M ;
DONLAN, P ;
BUFKIN, C ;
LIPTON, MJ .
JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY, 1995, 19 (03) :424-433
[4]
Liver microbubble transit time compared with histology and Child-Pugh score in diffuse liver disease: a cross sectional study [J].
Blomley, MJK ;
Lim, AKP ;
Harvey, CJ ;
Patel, N ;
Eckersley, RJ ;
Basilico, R ;
Heckemann, R ;
Urbank, A ;
Cosgrove, DO ;
Taylor-Robinson, SD .
GUT, 2003, 52 (08) :1188-1193
[5]
Complications of cirrhosis.: I.: Portal hypertension [J].
Bosch, J ;
García-Pagán, JC .
JOURNAL OF HEPATOLOGY, 2000, 32 :141-156
[6]
CONTRAST-ENHANCED NMR IMAGING - ANIMAL STUDIES USING GADOLINIUM-DTPA COMPLEX [J].
BRASCH, RC ;
WEINMANN, HJ ;
WESBEY, GE .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1984, 142 (03) :625-630
[7]
CRAIG JR, 1990, ANDERSONS PATHOLOGY, P1199
[8]
Early changes in liver perfusion caused by occult metastases in rats:: Detection with quantitative CT [J].
Cuenod, CA ;
Leconte, I ;
Siauve, N ;
Resten, A ;
Dromain, C ;
Poulet, B ;
Frouin, F ;
Clément, O ;
Frija, G .
RADIOLOGY, 2001, 218 (02) :556-561
[9]
DEFRANCQ J, 1993, ACTA RADIOL, V34, P478
[10]
FLEMING JS, 1983, J NUCL MED, V24, P1108