Srinivasan S, Krouskop T, Ophir J
Siemens Ultrasound Division, Siemens Medical Solutions, Mountain View, CA, USA.
Ultrasound Med Biol. 2004 Jul;30(7):899-918. doi: 10.1016/j.ultrasmedbio.2004.05.005.
Tissue stiffness is generally known to be associated with pathologic changes. Ultrasound (US) elastography, on the other hand, is capable of imaging tissue strain, which may or may not be well-correlated with tissue stiffness. Hence, a quantitative comparison between the elastographic tissue strain images and the corresponding tissue modulus images needed to be performed to evaluate the usefulness of elastography in imaging tissue stiffnesss properties. Simulations were performed to demonstrate and quantify the similarities between modulus images and strain elastograms. This was followed by comparing nanoindenter-based modulus images with strain elastograms of thin slices of tissue-mimicking phantoms. Finally, some beef slices, canine prostates, ovine kidneys and breast cancers grown in mice were used to demonstrate the qualitative correspondence between modulus images and strain elastograms. The simulations and the experiments indicated that it is feasible to perform quantitative comparisons between strain images (using elastography) and modulus images on certain tissue structures and geometries. A good quantitative correspondence (correlation values of greater than 0.8) between structures in the modulus and strain images could be obtained at scales equal to or larger than 20 Qlambda (where Q is the quality factor defined as the ratio of the center frequency over the band width and lambda is the wavelength of the US system) modulus contrasts larger than 5, applied strains between 0.5% and 3% and window lengths for computing strain elastograms between 3 Qlambda and 5 Qlambda. The gelatin-phantom experiments showed lower values of correlation (values around 0.5) than with theory and simulations. The decrease in correlation was attributed to the presence of measurement noise in both strain elastography and modulus imaging, an increase of dimensionality of the problem (from 2-D to 3-D), local anisotropy, heterogeneity and nonstationarity. Experiments on real tissue slices showed further decrease in the correlation to around 0.3, possibly due to additional confounding factors such as time-dependent mechanical properties and geometrical distortions in the tissue during imaging. The work presented in this paper demonstrates that there is an intrinsic relationship between strain elastograms and the actual distribution of soft tissue elastic moduli, and bodes well for continued work in the area of elastography.
组织硬度通常被认为与病理变化相关。另一方面,超声(US)弹性成像能够对组织应变进行成像,而这种应变可能与组织硬度有良好的相关性,也可能没有。因此,需要对弹性成像组织应变图像和相应的组织模量图像进行定量比较,以评估弹性成像在成像组织硬度特性方面的有用性。进行了模拟以证明并量化模量图像和应变弹性图之间的相似性。接下来将基于纳米压痕的模量图像与组织模拟体模薄片的应变弹性图进行比较。最后,使用一些牛肉片、犬前列腺、羊肾脏以及在小鼠体内生长的乳腺癌来证明模量图像和应变弹性图之间的定性对应关系。模拟和实验表明,在某些组织结构和几何形状上,对(使用弹性成像的)应变图像和模量图像进行定量比较是可行的。在等于或大于20Qλ(其中Q是定义为中心频率与带宽之比的品质因数,λ是超声系统的波长)的尺度、大于5的模量对比度、0.5%至3%的施加应变以及用于计算应变弹性图的3Qλ至5Qλ的窗口长度条件下,模量图像和应变图像中的结构之间可以获得良好的定量对应关系(相关值大于0.8)。明胶体模实验显示相关性值(约为0.5)低于理论和模拟值。相关性的降低归因于应变弹性成像和模量成像中均存在测量噪声、问题维度的增加(从二维到三维)、局部各向异性、不均匀性和非平稳性。对真实组织切片的实验表明相关性进一步降低至约0.3,这可能是由于诸如成像过程中组织随时间变化的力学性能和几何变形等额外的混杂因素所致。本文所呈现的工作表明,应变弹性图与软组织弹性模量的实际分布之间存在内在关系,这为弹性成像领域的持续研究奠定了良好基础。