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用于上皮癌诊断的漫反射光谱中半无限肿瘤模型的有效性:一项蒙特卡罗研究。

Validity of the semi-infinite tumor model in diffuse reflectance spectroscopy for epithelial cancer diagnosis: a Monte Carlo study.

作者信息

Zhu Caigang, Liu Quan

机构信息

Division of Bioengineering, School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore, Singapore.

出版信息

Opt Express. 2011 Aug 29;19(18):17799-812. doi: 10.1364/OE.19.017799.

Abstract

The accurate understanding of optical properties of human tissues plays an important role in the optical diagnosis of early epithelial cancer. Many inverse models used to determine the optical properties of a tumor have assumed that the tumor was semi-infinite, which infers infinite width and length but finite thickness. However, this simplified assumption could lead to large errors for small tumor, especially at the early stages. We used a modified Monte Carlo code, which is able to simulate light transport in a layered tissue model with buried tumor-like targets, to investigate the validity of the semi-infinite tumor assumption in two common epithelial tissue models: a squamous cell carcinoma (SCC) tissue model and a basal cell carcinoma (BCC) tissue model. The SCC tissue model consisted of three layers, i.e. the top epithelium, the middle tumor and the bottom stroma. The BCC tissue model also consisted of three layers, i.e. the top epidermis, the middle tumor and the bottom dermis. Diffuse reflectance was simulated for two common fiber-optic probes. In one probe, both source and detector fibers were perpendicular to the tissue surface; while in the other, both fibers were tilted at 45 degrees relative to the normal axis of the tissue surface. It was demonstrated that the validity of the semi-infinite tumor model depends on both the fiber-optic probe configuration and the tumor dimensions. Two look-up tables, which relate the validity of the semi-infinite tumor model to the tumor width in terms of the source-detector separation, were derived to guide the selection of appropriate tumor models and fiber optic probe configuration for the optical diagnosis of early epithelial cancers.

摘要

准确理解人体组织的光学特性在早期上皮癌的光学诊断中起着重要作用。许多用于确定肿瘤光学特性的反演模型都假定肿瘤是半无限大的,即宽度和长度无限但厚度有限。然而,这种简化假设对于小肿瘤可能会导致较大误差,尤其是在早期阶段。我们使用了一种改进的蒙特卡罗代码,它能够模拟光在具有埋藏肿瘤样目标的分层组织模型中的传输,以研究半无限大肿瘤假设在两种常见上皮组织模型中的有效性:鳞状细胞癌(SCC)组织模型和基底细胞癌(BCC)组织模型。SCC组织模型由三层组成,即顶部上皮、中间肿瘤和底部基质。BCC组织模型也由三层组成,即顶部表皮、中间肿瘤和底部真皮。针对两种常见的光纤探头模拟了漫反射率。在一种探头中,源光纤和探测器光纤都垂直于组织表面;而在另一种探头中,两根光纤都相对于组织表面的法线轴倾斜45度。结果表明,半无限大肿瘤模型的有效性取决于光纤探头配置和肿瘤尺寸。得出了两个查找表,它们将半无限大肿瘤模型的有效性与源探测器间距方面的肿瘤宽度联系起来,以指导为早期上皮癌的光学诊断选择合适的肿瘤模型和光纤探头配置。

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