虚拟可视化:混合数据梯度模型,在3D渲染中更准确地显示薄骨

IF 0.8 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Wolf Schweitzer , Michael Thali , Eloisa Aldomar
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引用次数: 0

摘要

计算机断层扫描(CT)和死后数据CT(PMCT)的传统3D渲染方法有时似乎不够真实,尤其是对于相对较薄的骨骼。当对完整的解剖结构进行成像并考虑面部或颞骨的骨折时,这可能是一个问题,其中可以看到缺陷或孔洞,而不是薄骨结构。这方面的技术问题是,目前使用的所有可视化方法(体积渲染、电影渲染和粒子跟踪、着色表面和等表面)都是由CT密度阈值定义的,而用户至少隐含地期望骨骼具有一定的最小密度CT。然而,一些骨骼区域,通常是骨骼相对较薄的区域,不满足这些期望,并且降低可视化阈值会导致在渲染图像中看到各种非骨组织。为了提供更真实的骨PMCT可视化,我们确定了一个混合数据梯度模型,该模型通过增加低密度骨区域(而不是非骨组织)的CT密度来改进CT数据。对于其他未修改的体积渲染,这将提供更令人满意的结果。作为3D渲染前的预处理,使用硬内核和软内核数据来获得3D密度图,使用3×3×3内核作为3D梯度图来确定灰度共生矩阵,然后将它们组合起来,以获得混合数据的最终梯度模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Virtopsy visualisation: Mixed data gradient model for more accurate thin bone visualization in 3D rendering

Conventional 3D rendering methods of computed tomography (CT) as well as post-mortem data CT (PMCT) sometimes do not seem to be authentic enough, especially for relatively thin bones. This can be a problem when imaging intact anatomy and considering fractures of the facial or temporal bones, where defects or holes may be visualized instead of thin bone structures. The technical aspect of this is that all currently used visualization methods (volume rendering, cinematic rendering and particle tracing, shaded surfaces and iso-surfaces) are defined by a CT-density threshold, whereas the user at least implicitly expects the bone to have a certain minimum density CT. However, some bone regions, typically those with relatively thin bone, do not meet these expectations, and lowering the threshold for visualization then results in all sorts of non-bone tissue being seen in the rendered images. To provide a more authentic PMCT visualization of bone, we identified a mixed data gradient model that improves the data from CT by increasing the CT density of low-density bone regions (but not of non-bone tissues). That delivers more satisfactory results for otherwise unmodified volume rendering. As pre-processing before 3D rendering, both hard and soft kernel data are used to obtain a 3D density map, a grayscale co-occurrence matrix is determined using a 3×3×3 kernel as the 3D gradient map, and these are then combined to obtain the final gradient model for mixed data.

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来源期刊
Forensic Imaging
Forensic Imaging RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
CiteScore
2.20
自引率
27.30%
发文量
39
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