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首页> 外文期刊>Brain imaging and behavior >A rare case of cerebellar agenesis: a probabilistic Constrained Spherical Deconvolution tractographic study
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A rare case of cerebellar agenesis: a probabilistic Constrained Spherical Deconvolution tractographic study

机译:小脑发育不全的罕见情况:概率约束球面反卷积术式研究

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Aim of this study is to show the potential of probabilistic tractographic techniques, based on the Constrained Spherical Deconvolution (CSD) algorithms, in recognizing white matter fiber bundle anomalies in patients with complex cerebral malformations, such as cerebellar agenesis. The morphological and tractographic study of a 17-year-old male patient affected by cerebellar agenesis was performed by using a 3Tesla MRI scanner. Genetic and neuropsychological tests were carried out. An MRI morphological study showed the absence of both cerebellar hemispheres and the flattening of the anterior side of the pons. Moreover, it showed a severe vermian hypoplasia with a minimal vermian residual. The study recognized two thin cerebellar remnants, medially in contact with the small vermian residual, at the pontine level. The third ventricle, morphologically normal, communicated with a permagna cerebello-medullary cistern. Probabilistic CSD tractography identified some abnormal and aberrant infratentorial tracts, symmetrical on both sides. In particular, the transverse pontine fibers were absent and the following tracts with aberrant trajectories have been identified: "cerebello-thalamic" tracts; "fronto-cerebellar" tracts; and ipsilateral and contralateral "spino-cerebellar" tracts. Abnormal tracts connecting the two thin cerebellar remnants have also been detected. There were no visible alterations in the main supratentorial tracts in either side. Neuropsychiatric evaluation showed moderate cognitive-motor impairment with discrete adaptive compensation. Probabilistic CSD tractography is a promising technique that overcome reconstruction biases of other diffusion tensor-based approaches and allowed us to recognize, in a patient with cerebellar agenesis, abnormal tracts and aberrant trajectories of normally existing tracts.
机译:这项研究的目的是展示基于约束球面反卷积(CSD)算法的概率性tractography技术在识别复杂脑畸形(例如小脑发育不全)患者的白质纤维束异常中的潜力。使用3Tesla MRI扫描仪对一名17岁男性小脑发育不全的男性患者进行了形态学和影像学研究。进行了遗传和神经心理学测试。 MRI形态学研究显示,既没有小脑半球,也没有脑桥前侧的扁平。而且,它显示出严重的Vermian发育不全,具有最小的Vermian残留。研究发现在桥脑水平上有两个细小脑残余物,中间与小Vermian残余物接触。第三脑室,形态正常,与permagna cerebello-髓水箱相通。概率性CSD超声检查可发现一些异常且异常的下胆道,两侧对称。特别是,缺少桥脑横纤维,并且已经鉴定出以下具有异常轨迹的道:“小脑-丘脑”道; “额小脑”区;以及同侧和对侧的“脊柱小脑”。还发现了连接两个薄小脑残余物的异常道。两侧主要的幕上肌无明显改变。神经精神病学评估显示中度认知运动障碍和离散适应性补偿。概率CSD体表学是一种有前途的技术,它可以克服其他基于扩散张量的方法的重建偏差,并允许我们在具有小脑发育不全的患者中识别正常存在的管束的异常管束和异常轨迹。

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