Liver Cancer
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jun 15, 2004; 10(12): 1730-1734
Published online Jun 15, 2004. doi: 10.3748/wjg.v10.i12.1730
Microvessel density of malignant and benign hepatic lesions and MRI evaluation
Jian-Ping Lu, Jian Wang, Tao Wang, Yi Wang, Wei-Qing Wu, Li Gao
Jian-Ping Lu, Jian Wang, Department of Radiology, Changhai Hospital, Second Military Medical University, Shanghai 200433, China
Tao Wang, Yi Wang, Wei-Qing Wu, Eastern Hepatobiliary Surgery Institute, Second Military Medical University, Shanghai 200433, China
Li Gao, Department of Pathology, Changhai Hospital, Second Military Medical University, Shanghai 200433, China
Author contributions: All authors contributed equally to the work.
Supported by the National Natural Science Foundation of China, No. 39970728
Correspondence to: Dr. Jian-Ping Lu, Department of Radiology, Changhai Hospital, Second Military Medical University, Shanghai 200433, China
Telephone: +86-21-25072133
Received: August 23, 2003
Revised: October 5, 2003
Accepted: October 12, 2003
Published online: June 15, 2004
Abstract

AIM: To study the difference of microvessel density (MVD) between malignant and benign hepatic lesions and study the relationship between MVD and dynamic enhanced magnetic resonance imaging (MRI) for evaluation of microvessels within malignant and benign hepatic lesions.

METHODS: A total of 265 specimens of hepatocellular carcinoma (HCC), 122 cirrhosis tissues and 22 hepatic benign lesions were enrolled for MVD by immunohistochemistry on tissue microarray, of which 49 underwent MRI examination before surgery, then contrast-to-noise ratios (CNR) and enhancement index (EI) in all the phases were calculated. Pearson correlation was performed for correlation analysis between CNR, EI and MVD.

RESULTS: MVD of HCC was 22.7 ± 15.8 (mean ± SD), which was obviously higher than that of cirrhosis tissue (8.3 ± 7.6, P < 0.01), but was not statistically different from that of benign lesions (31.3 ± 22.7, P>0.05). Among HCC, MVD of gradesI-II was 29.9 ± 18.6, which was much higher than those of grade III (22.2 ± 18.2, P < 0.01) and gradeIV (22.9 ± 19.0, P < 0.01). MVD of HCC (P = 0.018) and of benign lesions (P = 0.014) were both correlative with CNR in arterial phase.

CONCLUSION: Neoangiogenesis is an important feature for malignant tumor, and MVD may act as a biological marker in differentiating malignant from benign hepatic lesions. Dynamic enhanced MRI, especially image in arterial phase, may act as an MVD evaluation criterion for malignant and benign hepatic lesions.

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