基于迭代阈值法的数字减影血管造影图像中动静脉畸形病灶和血管的分割

Yuxi Lian, Yuanyuan Wang, Jinhua Yu, Yi Guo, Liang Chen
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引用次数: 5

摘要

数字减影血管造影(DSA)在血管疾病的诊断和治疗中发挥着重要作用。DSA图像中病灶和血管的分割是诊断动静脉畸形(AVM)的重要步骤。本文提出了一种基于全局和迭代局部阈值分割的DSA图像病灶和血管分割方法。首先,将原始图像分割成适当的子图像。对于每个子图像,主要使用Ostu的方法,并通过阈值将像素分为两组。然后,根据子图像强度的方差,计算两组像素的均值或中值,将像素分为三类。这三类分别代表原始DSA图像中的暗AVM和血管、亮背景和未确定区域。前两个类是直接确定的,不会被进一步处理。在下一次迭代中处理未确定的区域以分割微血管,直到两次迭代之间的阈值小于预设的阈值。最后,将所有类组合在一起创建分割结果。我们在AVM的DSA图像上测试了该方法。实验结果表明,该方法对DSA图像的分割效果优于现有的分割方法。该方法既能识别细小血管结构,又能在同一框架内识别较大的AVM病灶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Segmentation of arteriovenous malformations nidus and vessel in digital subtraction angiography images based on an iterative thresholding method
Digital subtraction angiography (DSA) plays an important role in the diagnosis and therapy of vascular diseases. Segmentation of nidus and vessel in DSA images is an essential step in the diagnosis of arteriovenous malformations (AVM). In this paper, a novel segmentation method based on the global and iterative local thresholding is proposed to segment the nidus and vessel in DSA images. Firstly, the original image is divided into proper subimages. For each subimage, Ostu's method is primarily used and pixels are classified into two groups by the threshold. Then, according to the variance of the subimage intensities, the mean or median values of two groups are calculated to sort the pixels into three classes. These three classes represent the dark AVM and vessel, the bright background and undetermined regions in the original DSA image. The first two classes are determined directly and will not be processed further. The undetermined regions are processed in the next iteration to segment tiny vessels until the thresholds between two iterations are less than a preset one. Finally, all classes are combined to create the segmentation result. We test this method on DSA images of the AVM. Experimental results show that the proposed method performs better than the other state-of-the-art methods in the segmentation of DSA images. The proposed method can identify fine and tiny vessel structures, as well as distinguish large AVM nidus in one framework.
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