Parisot Sarah, Duffau Hugues, Chemouny Stéphane, Paragios Nikos
Laboratoire MAS, Ecole Centrale Paris, Chatenay Malabry, France.
Med Image Comput Comput Assist Interv. 2011;14(Pt 2):508-15. doi: 10.1007/978-3-642-23629-7_62.
Low-grade gliomas (WHO grade II) are diffusively infiltrative brain tumors arising from glial cells. Spatial classification that is usually based on cerebral lobes lacks accuracy and is far from being able to provide some pattern or statistical interpretation of their appearance. In this paper, we propose a novel approach to understand and infer position of low-grade gliomas using a graphical model. The problem is formulated as a graph topology optimization problem. Graph nodes correspond to extracted tumors and graph connections to the spatial and content dependencies among them. The task of spatial position mapping is then expressed as an unsupervised clustering problem, where cluster centers correspond to centers with position appearance prior, and cluster samples to nodes with strong statistical dependencies on their position with respect to the cluster center. Promising results using leave-one-out cross-validation outperform conventional dimensionality reduction methods and seem to coincide with conclusions drawn in physiological studies regarding the expected tumor spatial distributions and interactions.
低级别胶质瘤(世界卫生组织二级)是起源于神经胶质细胞的弥漫性浸润性脑肿瘤。通常基于脑叶的空间分类缺乏准确性,远远无法对其外观提供某种模式或统计解释。在本文中,我们提出了一种使用图形模型来理解和推断低级别胶质瘤位置的新方法。该问题被表述为一个图拓扑优化问题。图节点对应于提取的肿瘤,图连接对应于它们之间的空间和内容依赖性。然后,空间位置映射任务被表示为一个无监督聚类问题,其中聚类中心对应于具有位置外观先验的中心,聚类样本对应于在其相对于聚类中心的位置上具有强统计依赖性的节点。使用留一法交叉验证得到的有前景的结果优于传统的降维方法,并且似乎与生理学研究中关于预期肿瘤空间分布和相互作用得出的结论一致。