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Clustering multidimensional MR images to detect metabolic changes in different tissue classes

机译:聚类多维MR图像检测不同组织类的代谢变化

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A tissue database was established by using multidimensional clusters of exact longitudinal (T$- 1$/) and transversal (T$-2$/) relaxation times and spin density, allowing the automatic segmentation and characterization of healthy and pathologic tissue. All parameters were simultaneously acquired employing a modified Multi-Echo pulse sequence. Initial clinical results showed a good differentiation between normal brain tissue and pathologic tissue like edema and meningioma. Inhomogeneous tumors such as high-grade glioblastoma were difficult to characterize automatically. The implementation of a diffusion-weighted modified Tanner-Stejskal pulse sequence allows the acquisition of the Apparent Diffusion Constant (ADC), which has been incorporated for the first time into a multidimensional information set as a new tissue-characterizing parameter. This parameter is sensitive to changes in the mobility of water in and between different cell compartments resulting from metabolic cell disorders like ischemic or edematous processes. To reproduce the known results of animal experiments, where as early as 30 min after an ischemic event the measurement of the ADC led to a diagnosis, diffusion-weighted imaging had to be implemented on a standard clinical scanner. The correction of unavoidable motion artifacts, which occur when applying diffusion- weighted spin echo sequences on standard clinical scanners, require the implementation of a special sequence using the navigator echo method followed by a correction algorithm of the raw data in Fourier space. Initial results showed a significant improvement in the differentiation of healthy and pathologic tissue classes.
机译:和横向(T $ -2 $ /)的弛豫时间和自旋密度,从而使健康的和病理组织的自动分割和表征 - 甲组织数据库通过使用精确纵向($ 1 / T $)的多维集群建立。所有参数都同时获得采用一种改进的多回波脉冲序列。初步临床结果显示正常脑组织和病理组织像水肿和脑膜瘤之间具有良好的分化。不均匀的肿瘤如高档胶质母细胞瘤是很难自动表征。一个扩散加权改性唐纳-Stejskal脉冲序列的实现允许采集表观扩散常数(ADC),其中已掺入首次成多维信息组作为新的组织表征参数的。该参数是在水和在从等缺血性或水肿过程代谢细胞疾病导致不同的细胞区室之间的迁移率的变化很敏感。要重现的动物实验,其中早30分钟缺血事件导致了诊断ADC的测量后,扩散加权成像必须在标准临床扫描仪实现的已知结果。不可避免的运动伪影,施加在标准的临床扫描仪弥散加权的自旋回波序列时出现的校正,需要使用导航回波方法,接着在傅立叶空间中的原始数据的校正算法特殊序列的执行。初步结果显示,在健康和病理组织阶级的分化显著的改善。

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