Maity Santanu, Alrubayan Mousa, Pradhan Prabhakar
Department of Physics and Astronomy, Mississippi State University, Mississippi State, MS, USA, 39762.
ArXiv. 2025 May 27:arXiv:2505.21080v1.
We explored the fractal and multifractal characteristics of breast mammogram micrographs to identify quantitative biomarkers associated with breast cancer progression. In addition to conventional fractal and multifractal analyses, we employed a recently developed fractal-functional distribution method, which transforms fractal measures into Gaussian distributions for more robust statistical interpretation. Given the sparsity of mammogram intensity data, we also analyzed how variations in intensity thresholds, used for binary transformations of the fractal dimension, follow unique trajectories that may serve as novel indicators of disease progression. Our findings demonstrate that fractal, multifractal, and fractal-functional parameters effectively differentiate between benign and cancerous tissue. Furthermore, the threshold-dependent behavior of intensity-based fractal measures presents distinct patterns in cancer cases. To complement these analyses, we applied the Inverse Participation Ratio (IPR) light localization technique to quantify structural disorder at the microscopic level. This multi-parametric approach, integrating spatial complexity and structural disorder metrics, offers a promising framework for enhancing the sensitivity and specificity of breast cancer detection.
我们探究了乳腺钼靶显微图像的分形和多重分形特征,以识别与乳腺癌进展相关的定量生物标志物。除了传统的分形和多重分形分析外,我们还采用了一种最近开发的分形功能分布方法,该方法将分形测量值转换为高斯分布,以便进行更稳健的统计解释。鉴于钼靶强度数据的稀疏性,我们还分析了用于分形维数二元变换的强度阈值变化如何遵循独特轨迹,这些轨迹可能作为疾病进展的新指标。我们的研究结果表明,分形、多重分形和分形功能参数能够有效区分良性和癌性组织。此外,基于强度的分形测量的阈值依赖性行为在癌症病例中呈现出不同的模式。为了补充这些分析,我们应用了逆参与率(IPR)光定位技术来量化微观层面的结构无序。这种整合空间复杂性和结构无序指标的多参数方法,为提高乳腺癌检测的灵敏度和特异性提供了一个有前景的框架。