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首页> 外文期刊>Micron: The international research and review journal for microscopy >Quantifying the architectural complexity of microscopic images of histology specimens
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Quantifying the architectural complexity of microscopic images of histology specimens

机译:量化组织学标本显微图像的建筑复杂性

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Tumour grade (a measure of the degree of cellular differentiation of malignant neoplasm) is an important prognostic factor in many types of cancer. In general, poorly differentiated tumours are characterized by a higher degree of architectural irregularity and complexity of histological structures. Fractal dimension is a useful parameter for characterizing complex irregular structures. However, one of the difficulties of estimating the fractal dimension from microscopic images is the segmentation of pathologically relevant structures for analysis. A commonly used technique to segment structures of interest is to apply a pixel intensity threshold to convert the original image to binary and extract pixel outline structures from the binary representation. The difficulty with this approach is that the value of the threshold required to segment the histological structures is highly dependent on the staining technique chosen and imaging conditions (i.e., illumination time, intensity, and uniformity) of the microscopic system. In this work, we present a method for finding the optimal intensity threshold by maximizing the corresponding fractal dimension. This method results in the segmentation of histological structures and the estimation of their fractal dimension (independent of imaging conditions). We applied our technique to 164 prostate histology sections from 82 prostate core biopsy specimens (two serial sections from each of the 63 benign prostate tissues and 19 high grade prostate carcinoma). We stained one of the serial sections with conventional hemotoxylin and eosin (H&E) and the other with pan-keratin, and found that the difference in mean fractal dimension between the two groups was statistically significant (p < 0.0001) for both stains. However, using receiver operating characteristics (ROC) analysis, we conclude that our fractal dimension method applied to the images of pan-keratin stained sections provides greater classification performance (benign versus high grade) than with those stained with H&E when compared to the original histological diagnosis. The sensitivity and specificity achieved with the pan-keratin images were 89.5% and 90.5%, respectively.
机译:肿瘤等级(衡量恶性肿瘤细胞分化程度的指标)是许多类型癌症的重要预后因素。通常,低分化肿瘤的特征在于较高的结构不规则性和组织学结构的复杂性。分形维数是表征复杂不规则结构的有用参数。然而,从显微图像估计分形维数的困难之一是对病理相关结构进行分割以进行分析。分割感兴趣的结构的常用技术是应用像素强度阈值,以将原始图像转换为二进制,并从二进制表示中提取像素轮廓结构。这种方法的困难在于,分割组织结构所需的阈值高度取决于所选择的染色技术和显微系统的成像条件(即照明时间,强度和均匀性)。在这项工作中,我们提出了一种通过最大化相应的分形维数来找到最佳强度阈值的方法。该方法导致组织结构的分割和其分形维数的估计(与成像条件无关)。我们将我们的技术应用于82例前列腺核心活检标本中的164例前列腺组织学切片(63个良性前列腺组织和19例高等级前列腺癌各取两个连续切片)。我们用常规的苏木精和曙红(H&E)染色了一系列切片,而用泛角蛋白染色了另一部分,发现两组之间的平均分形维数差异在统计学上均具有统计学意义(p <0.0001)。但是,使用接收器操作特征(ROC)分析,我们得出的结论是,与原始组织学相比,应用于泛角蛋白染色切片图像的分形维数方法提供的分类性能(良性与高品位)要好于H&E染色诊断。使用全角蛋白图像获得的敏感性和特异性分别为89.5%和90.5%。

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