Focal liver lesions: multiparametric microvasculature characterization via super-resolution ultrasound imaging

被引:0
作者
Zeng, Qian-Qian [1 ,2 ]
An, Shi-Zhe [3 ]
Chen, Chao-Nan [1 ,2 ]
Wang, Zhen [1 ,2 ]
Liu, Jia-Cheng [3 ]
Wan, Ming-Xi [3 ]
Zong, Yu-Jin [3 ]
Jian, Xiao-Hua [4 ]
Yu, Jie [1 ]
Liang, Ping [1 ]
机构
[1] Peoples Liberat Army Gen Hosp, Dept Intervent Ultrasound, Sr Dept Oncol, Med Ctr 5, Beijing 100853, Peoples R China
[2] Chinese Peoples Liberat Army PLA, Med Sch, Beijing 100853, Peoples R China
[3] Xi An Jiao Tong Univ, Key Lab Biomed Informat Engn, Minist Educ, Dept Biomed Engn,Sch Life Sci & Technol, Xian 710049, Peoples R China
[4] Nanjing Univ, Sch Mat Sci & Intelligent Engn, Suzhou 215163, Peoples R China
基金
中国国家自然科学基金;
关键词
Carcinoma (hepatocellular); Focal nodular hyperplasia; Liver neoplasms; Microbubbles; Ultrasonography; LOCALIZATION MICROSCOPY; NODULAR HYPERPLASIA; CT; US;
D O I
10.1186/s41747-024-00540-3
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
Background Noninvasive and functional imaging of the focal liver lesion (FLL) vasculature at microscopic scales is clinically challenging. We investigated the feasibility of using super-resolution ultrasound (SR-US) imaging for visualizing and quantifying the microvasculature of intraparenchymal FLLs. Methods Patients with FLLs between June 2022 and February 2023 were prospectively screened. Following bolus injection of microbubbles at clinical concentration, SR-US was performed using a high frame rate (350-500 Hz) modified ultrasound scanner and a convex array transducer with a central frequency of 3.1 MHz. Results In total, 47 pathologically proven FLLs at a depth of 5.7 +/- 1.7 cm (mean +/- standard deviation) were included: 30 hepatocellular carcinomas (HCC), 11 liver metastases (LM), and 6 focal nodular hyperplasias (FNH). The smallest detectable vessel size of the hepatic microvasculature was 128.4 +/- 18.6 mu m (mean +/- standard deviation) at a depth of 8 cm. Significant differences were observed among the three types of lesions in terms of pattern categories, vessel density, minimum flow velocity, and perfusion index. We observed higher vessel density for FNH versus liver parenchyma (p < 0.001) as well as fractal dimension and local flow direction entropy value for FNH versus HCC (p = 0.002 and p < 0.001, respectively) and for FNH versus LM (p = 0.006 and p = 0.002, respectively). Conclusion Multiparametric SR-US showed that these three pathological types of FLLs have specific microvascular phenotypes. Vessel density, fractal dimension and local flow direction entropy served as valuable parameters in distinguishing between benign and malignant FLLs.
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页数:14
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