A Generative Probabilistic Model and Discriminative Extensions for Brain Lesion Segmentation- With Application to Tumor and Stroke

被引:66
作者
Menze, Bjoern H. [1 ,2 ,3 ,4 ,5 ]
Van Leemput, Koen [6 ,7 ]
Lashkari, Danial [1 ]
Riklin-Raviv, Tammy [8 ]
Geremia, Ezequiel [2 ]
Alberts, Esther [4 ,5 ]
Gruber, Philipp [9 ]
Wegener, Susanne [9 ]
Weber, Marc-Andre [10 ]
Szekely, Gabor [3 ]
Ayache, Nicholas [2 ]
Golland, Polina [1 ]
机构
[1] MIT, Comp Sci & Artificial Intelligence Lab, Cambridge, MA 02139 USA
[2] INRIA Sophia Antipolis, Asclepios Res Project, F-06902 Sophia Antipolis, France
[3] ETH, Comp Vis Lab, CH-8092 Zurich, Switzerland
[4] Tech Univ Munich, Inst Adv Study, D-80333 Munich, Germany
[5] Tech Univ Munich, Dept Comp Sci, D-80333 Munich, Germany
[6] Harvard Univ, Dept Radiol, Massachusetts Gen Hosp, Sch Med, Charlestown, MA 02129 USA
[7] Tech Univ Denmark, Dept Appl Math & Comp Sci, DK-2800 Lyngby, Denmark
[8] Ben Gurion Univ Negev, Dept Elect & Comp Engn, IL-8410501 Beer Sheva, Israel
[9] Univ Zurich Hosp, Dept Neurol, CH-8091 Zurich, Switzerland
[10] Univ Heidelberg Hosp, Dept Diagnost Radiol, D-69120 Heidelberg, Germany
基金
欧洲研究理事会;
关键词
Terms Medical diagnostic imaging; anatomical structure; tumors; image segmentation; object segmentation; Bayes methods; DEFORMABLE REGISTRATION; BAYESIAN MODEL; FRAMEWORK; FORESTS; GROWTH; IMAGES;
D O I
10.1109/TMI.2015.2502596
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
We introduce a generative probabilistic model for segmentation of brain lesions in multi-dimensional images that generalizes the EM segmenter, a common approach for modelling brain images using Gaussian mixtures and a probabilistic tissue atlas that employs expectation-maximization (EM), to estimate the label map for a new image. Our model augments the probabilistic atlas of the healthy tissues with a latent atlas of the lesion. We derive an estimation algorithm with closed-form EM update equations. The method extracts a latent atlas prior distribution and the lesion posterior distributions jointly from the image data. It delineates lesion areas individually in each channel, allowing for differences in lesion appearance across modalities, an important feature of many brain tumor imaging sequences. We also propose discriminative model extensions to map the output of the generative model to arbitrary labels with semantic and biological meaning, such as "tumor core" or "fluid-filled structure", but without a one-to-one correspondence to the hypo- or hyper-intense lesion areas identified by the generative model. We test the approach in two image sets: the publicly available BRATS set of glioma patient scans, and multi modal brain images of patients with acute and subacute ischemic stroke. We find the generative model that has been designed for tumor lesions to generalize well to stroke images, and the extended discriminative-discriminative model to be one of the top ranking methods in the BRATS evaluation.
引用
收藏
页码:933 / 946
页数:14
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