Back to Search Start Over

Robust Multicontrast MRI Spleen Segmentation for Splenomegaly Using Multi-Atlas Segmentation

Authors :
Richard G. Abramson
Albert Assad
Yuankai Huo
Zhoubing Xu
Jiaqi Liu
Bennett A. Landman
Robert L. Harrigan
Source :
IEEE Transactions on Biomedical Engineering. 65:336-343
Publication Year :
2018
Publisher :
Institute of Electrical and Electronics Engineers (IEEE), 2018.

Abstract

Objective: Magnetic resonance imaging (MRI) is an essential imaging modality in noninvasive splenomegaly diagnosis. However, it is challenging to achieve spleen volume measurement from three-dimensional MRI given the diverse structural variations of human abdomens as well as the wide variety of clinical MRI acquisition schemes. Multi-atlas segmentation (MAS) approaches have been widely used and validated to handle heterogeneous anatomical scenarios. In this paper, we propose to use MAS for clinical MRI spleen segmentation for splenomegaly. Methods: First, an automated segmentation method using the selective and iterative method for performance level estimation (SIMPLE) atlas selection is used to address the concerns of inhomogeneity for clinical splenomegaly MRI. Then, to further control outliers, semiautomated craniocaudal spleen length-based SIMPLE atlas selection (L-SIMPLE) is proposed to integrate a spatial prior in a Bayesian fashion and guide iterative atlas selection. Last, a graph cuts refinement is employed to achieve the final segmentation from the probability maps from MAS. Results: A clinical cohort of 55 MRI volumes (28 T1 weighted and 27 T2 weighted) was used to evaluate both automated and semiautomated methods. Conclusion: The results demonstrated that both methods achieved median Dice > 0.9, and outliers were alleviated by the L-SIMPLE (≈1 min manual efforts per scan), which achieved 0.97 Pearson correlation of volume measurements with the manual segmentation. Significance: In this paper, spleen segmentation on MRI splenomegaly using MAS has been performed.

Details

ISSN :
15582531 and 00189294
Volume :
65
Database :
OpenAIRE
Journal :
IEEE Transactions on Biomedical Engineering
Accession number :
edsair.doi.dedup.....f3c5a46b9085ab1d094666badbcd08ea
Full Text :
https://doi.org/10.1109/tbme.2017.2764752