Cellular microstructural parameters mapping can provide quantitative information for tumor diagnosis and treatment monitoring. Particularly, voxel-wise cell size distribution may provide critical clinical biomarkers to characterize heterogeneity of tumors. Currently, MRI-cytometry may measure such a distribution, but it “blurs” the distribution peaks and prevents differentiating different cell populations with different cell sizes. In this work, we develop a new approach to improve this and hence make it more practical to distinguish different cells. Detection of T cell infiltration for assessment of early response to immunotherapy may be a potential application of this method.
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