Diffusion-Weighted MRI Reflects Proliferative Activity in Primary CNS Lymphoma

To investigate if apparent diffusion coefficient (ADC) values within primary central nervous system lymphoma correlate with cellularity and proliferative activity in corresponding histological samples. Echo-planar diffusion-weighted magnetic resonance images obtained from 21 patients with primary ce...

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Published inPloS one Vol. 11; no. 8; p. e0161386
Main Authors Schob, Stefan, Meyer, Jonas, Gawlitza, Matthias, Frydrychowicz, Clara, Müller, Wolf, Preuss, Matthias, Bure, Lionel, Quäschling, Ulf, Hoffmann, Karl-Titus, Surov, Alexey
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 29.08.2016
Public Library of Science (PLoS)
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Summary:To investigate if apparent diffusion coefficient (ADC) values within primary central nervous system lymphoma correlate with cellularity and proliferative activity in corresponding histological samples. Echo-planar diffusion-weighted magnetic resonance images obtained from 21 patients with primary central nervous system lymphoma were reviewed retrospectively. Regions of interest were drawn on ADC maps corresponding to the contrast enhancing parts of the tumors. Biopsies from all 21 patients were histologically analyzed. Nuclei count, total nuclei area and average nuclei area were measured. The proliferation index was estimated as Ki-67 positive nuclei divided by total number of nuclei. Correlations of ADC values and histopathologic parameters were determined statistically. Ki-67 staining revealed a statistically significant correlation with ADCmin (r = -0.454, p = 0.038), ADCmean (r = -0.546, p = 0.010) and ADCmax (r = -0.515, p = 0.017). Furthermore, ADCmean correlated in a statistically significant manner with total nucleic area (r = -0.500, p = 0.021). Low ADCmin, ADCmean and ADCmax values reflect a high proliferative activity of primary cental nervous system lymphoma. Low ADCmean values-in concordance with several previously published studies-indicate an increased cellularity within the tumor.
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Conceptualization: SS AS UQ KTH. Data curation: SS AS KTH MG. Formal analysis: MG JM LB CF. Investigation: SS AS UQ. Methodology: SS AS UQ KTH CF LB. Project administration: AS KTH UQ WM. Resources: WM CF. Software: JM WM MP. Supervision: KTH UQ AS WM. Validation: MG JM MP LB. Visualization: SS AS UQ. Writing – original draft: SS AS. Writing – review & editing: SS AS.
Competing Interests: The authors have declared that no competing interests exist.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0161386