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首页> 外文期刊>Journal of neuro-oncology. >A multi-resolution textural approach to diagnostic neuropathology reporting
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A multi-resolution textural approach to diagnostic neuropathology reporting

机译:诊断神经病理学报告的多分辨率纹理方法

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We present a computer aided diagnostic workflow focusing on two diagnostic branch points in neuropathology (intraoperative consultation and p53 status in tumor biopsy specimens) by means of texture analysis via discrete wavelet frames decomposition. For intraoperative consultation, our methodology is capable of classifying glioblastoma versus metastatic cancer by extracting textural features from the non-nuclei region of cytologic preparations based on the imaging characteristics of glial processes, which appear as anisotropic thin linear structures. For metastasis, these are homogeneous in appearance, thus suitable and extractable texture features distinguish the two tissue types. Experiments on 53 images (29 glioblastomas and 24 metastases) resulted in average accuracy as high as 89.7 % for glioblastoma, 87.5 % for metastasis and 88.7 % overall. For p53 interpretation, we detect and classify p53 status by classifying staining intensity into strong, moderate, weak and negative sub-classes. We achieved this by developing a novel adaptive thresholding for detection, a two-step rule based on weighted color and intensity for the classification of positively and negatively stained nuclei, followed by texture classification to classify the positively stained nuclei into the strong, moderate and weak intensity sub-classes. Our detection method is able to correctly locate and distinguish the four types of cells, at 85 % average precision and 88 % average sensitivity rate. These classification methods on the other hand recorded 81 % accuracy in classifying the positive and negative cells, and 60 % accuracy in further classifying the positive cells into the three intensity groups, which is comparable with neuropathologists' markings.
机译:我们提出了一种计算机辅助的诊断工作流程,它通过离散小波框架分解的纹理分析,着重于神经病理学中的两个诊断分支点(术中会诊和肿瘤活检标本中的p53状态)。对于术中咨询,我们的方法能够根据胶质突的成像特征从细胞学制剂的非核区域提取纹理特征,从而将胶质母细胞瘤与转移性癌症进行分类,这些特征表现为各向异性的薄线性结构。对于转移,这些在外观上是均匀的,因此合适的和可提取的纹理特征区分了两种组织类型。对53张图像(29个胶质母细胞瘤和24个转移灶)进行的实验得出,胶质母细胞瘤的平均准确率高达89.7%,转移的准确率高达87.5%,总体准确率高达88.7%。对于p53解释,我们通过将染色强度分为强,中,弱和阴性亚类来检测和分类p53状态。我们通过开发一种新颖的自适应检测阈值,基于加权颜色和强度的两步法则来对正负染色核进行分类,然后通过纹理分类将正染色核分类为强,中和弱,从而实现了这一目标强度子类。我们的检测方法能够正确定位和区分四种类型的细胞,平均准确度为85%,平均敏感度为88%。另一方面,这些分类方法记录的将阳性细胞和阴性细胞分类的准确度为81%,将阳性细胞进一步分为三个强度组的准确度为60%,与神经病理学家的标记相当。

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