A Clifford Analytic Signal-Based Breast Lesion Segmentation Method for 4D Spatial-Temporal DCE-MRI Sequences

5Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Dynamic contrast enhanced magnetic resonance imaging (DCE-MRI) has been increasingly used for lesion detection in breast cancer diagnosis for its capability to provide spatial-temporal information. However, the massive and complex 4D spatial-temporal DCE-MRI data make the diagnosis process lengthy and error-prone. Moreover, normal fibroglandular tissue is occasionally enhanced through background parenchymal enhancement (BPE), which can degrade the performance of current algorithms. We propose a new method using a 3D Clifford analytic signal (CAS) approach for breast lesion segmentation of DCE-MRI data. A 2D temporal image is constructed from all the 2D DCE-MRI slices at different scanning time points on a given transverse plane, according to the CAS approach. Then, a 3D Clifford temporal image (CTI) is constructed by successively stacking temporal images. The proposed CTI can distinguish lesion regions both visually and quantitatively compared to the traditional DCE-MRI subtraction image. Finally, we employ a fully convolutional network (FCN) model for breast lesion segmentation using the CTI as one of the inputs. Experimental results on an independent public dataset (TCIA QIN breast DCE-MRI) and a private household breast DCE-MRI dataset (TBD) show that the proposed method can achieve superior performance over current methods, both qualitatively and quantitatively.

Cite

CITATION STYLE

APA

Wang, L., Shen, H., Zhang, J., Zhu, Y., & Jiang, C. (2020). A Clifford Analytic Signal-Based Breast Lesion Segmentation Method for 4D Spatial-Temporal DCE-MRI Sequences. IEEE Access, 8, 3901–3910. https://doi.org/10.1109/ACCESS.2019.2962750

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free