Virtual touch imaging quantification shear-wave elastography for breast lesions: the diagnostic value of qualitative and quantitative features

被引:4
作者
Luo, T. [1 ]
Zhang, J. W. [1 ]
Zhu, Y. [1 ]
Jia, X. H. [1 ]
Dong, Y. J. [1 ]
Zhan, W. W. [1 ]
Zhou, J. Q. [1 ]
机构
[1] Shanghai Jiao Tong Univ, Ruijin Hosp, Dept Ultrasound, Sch Med, Shanghai 200025, Peoples R China
基金
中国国家自然科学基金;
关键词
ACOUSTIC RADIATION FORCE; PATTERN-CLASSIFICATION; DIFFERENTIAL-DIAGNOSIS; CLINICAL-USE; DATA SYSTEM; ULTRASOUND; MASSES; BENIGN; US; ULTRASONOGRAPHY;
D O I
10.1016/j.crad.2020.10.016
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 investigate the value of the qualitative and quantitative features of Virtual Touch imaging quantification (VTIQ) shear-wave elastography in the characterisation of breast lesions. MATERIALS AND METHODS: Conventional ultrasound (US) and VTIQ were performed in 148 solid breast lesions in 148 women. During qualitative analysis, patterns of VTIQ were categorised into two patterns, 1 and 2. During quantitative analysis, the mean SWV (SWVmean) and the maximum SWV (SWVmax) of each lesion were used. The sensitivity, specificity, and the areas under the receiver operating characteristic (ROC) curve (Az value) were calculated for conventional US, VTIQ and combined conventional US and VTIQ. RESULTS: Malignant lesions were more likely to show VTIQ pattern 2 than the benign lesions (p<0.001). There was no significant difference in the Az values between SWVmean (0.907) and SWVmax (0.902; p=0.572). There was no significant difference in the Az values between the VTIQ pattern (0.884) and SWVmax (p=0.572). The combined conventional US and VTIQ pattern carried a similar Az value (0.949) as compared with the combined conventional US and SWVmax, which yielded an Az value of 0.952 (p=0.683). CONCLUSION: The combination of either VTIQ pattern or SWVmax and conventional US may be helpful in the characterisation of benign and malignant breast lesions. (C) 2020 The Royal College of Radiologists. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:316.e1 / 316.e8
页数:8
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