SpineParseNet: Spine Parsing for Volumetric MR Image by a Two-Stage Segmentation Framework With Semantic Image Representation

分割 人工智能 计算机科学 图像分割 图形 模式识别(心理学) 解析 计算机视觉 代表(政治) 理论计算机科学 政治学 政治 法学
作者
Shumao Pang,Chunlan Pang,Lei Zhao,Yangfan Chen,Zhihai Su,Yujia Zhou,Meiyan Huang,Wei Yang,Hai Lü,Qianjin Feng
出处
期刊:IEEE Transactions on Medical Imaging [Institute of Electrical and Electronics Engineers]
卷期号:40 (1): 262-273 被引量:170
标识
DOI:10.1109/tmi.2020.3025087
摘要

Spine parsing (i.e., multi-class segmentation of vertebrae and intervertebral discs (IVDs)) for volumetric magnetic resonance (MR) image plays a significant role in various spinal disease diagnoses and treatments of spine disorders, yet is still a challenge due to the inter-class similarity and intra-class variation of spine images. Existing fully convolutional network based methods failed to explicitly exploit the dependencies between different spinal structures. In this article, we propose a novel two-stage framework named SpineParseNet to achieve automated spine parsing for volumetric MR images. The SpineParseNet consists of a 3D graph convolutional segmentation network (GCSN) for 3D coarse segmentation and a 2D residual U-Net (ResUNet) for 2D segmentation refinement. In 3D GCSN, region pooling is employed to project the image representation to graph representation, in which each node representation denotes a specific spinal structure. The adjacency matrix of the graph is designed according to the connection of spinal structures. The graph representation is evolved by graph convolutions. Subsequently, the proposed region unpooling module re-projects the evolved graph representation to a semantic image representation, which facilitates the 3D GCSN to generate reliable coarse segmentation. Finally, the 2D ResUNet refines the segmentation. Experiments on T2-weighted volumetric MR images of 215 subjects show that SpineParseNet achieves impressive performance with mean Dice similarity coefficients of 87.32 ± 4.75%, 87.78 ± 4.64%, and 87.49 ± 3.81% for the segmentations of 10 vertebrae, 9 IVDs, and all 19 spinal structures respectively. The proposed method has great potential in clinical spinal disease diagnoses and treatments.
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