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. 2002 Apr;23(4):520-7.

Diffusion tensor MR imaging of high-grade cerebral gliomas

Saurabh Sinha  1 , Mark E Bastin, Ian R Whittle, Joanna M Wardlaw
Affiliations

Diffusion tensor MR imaging of high-grade cerebral gliomas

Saurabh Sinha et al. AJNR Am J Neuroradiol. 2002 Apr.

Abstract

Background and purpose: Optimizing high-grade glioma treatment requires the delineation of edematous and normal brain from tumor, perhaps by using potential differences in the absolute diffusion parameters of water. Our purpose was to determine whether mean diffusivity <D> and diffusion anisotropic MR imaging data help in this differentiation.

Methods: Nine patients with high-grade cerebral glioblastoma underwent contrast-enhanced structural and diffusion tensor MR imaging before therapy. Tumor, edematous brain, and apparently normal white matter regions were determined on T2-weighted and contrast-enhanced T1-weighted structural images. Fractional anisotropy (FA) and <D> were measured in each tissue type. Differences in these values among the tissue types were assessed with a standard analysis of variance.

Results: <D> was highest in the necrotic tumor core (1825.38 +/-404.06) x 10(-6) mm(2)/s, followed by edematous brain (1411.23 +/- 322.31) x 10(-6) mm(2)/s, enhancing tumor core (1308.67 +/- 292.50) x 10(-6) mm(2)/s, enhancing tumor margin (1229.80 +/- 206.80) x 10(-6) mm(2)/s, and normal brain (731.53 +/- 35.21) x 10(-6) mm(2)/s. FA was highest in normal brain (0.47 +/- 0.08) and lowest in the necrotic core (0.09 +/- 0.03). <D> was significantly different in enhancing tumor margins and edematous brain in all patients; FA was significantly different in only seven. These values were significantly different from those of normal brain in all cases in which they were measurable.

Conclusion: <D> values can be used to differentiate normal white matter, edematous brain, and enhancing tumor margins. Diffusion anisotropic data added no benefit to tissue differentiation. Further studies are required to determine if a <D> value that corresponds to the limit of tumor invasion can be identified.

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Figures

F<sc>ig</sc> 1.
Fig 1.
Images in patient 4. A and B, Contrast-enhanced T1-weighted volume images. In B, the solid arrow indicates a region of an enhancing tumor margin; dashed arrow, enhancing tumor core; dotted arrow, nonenhancing tumor core. C and D, T2-weighted EP images. Arrow in D indicates a region of edematous brain. E, 〈D〉 parametric map. F, FA parametric map.
F<sc>ig</sc> 2.
Fig 2.
Images in patient 5. A, Contrast-enhanced T1-weighted volume image. The solid arrow indicates a region of enhancing tumor margin; dashed arrow, enhancing tumor core; dotted arrow, nonenhancing tumor core. B, T2-weighted EP images. Arrow indicates a region of edematous brain. C and D, Note the high 〈D〉 and low FA values in the nonenhancing tumor core and edematous brain on the 〈D〉 parametric map (C) and FA parametric map (D).
F<sc>ig</sc> 3.
Fig 3.
Images in patient 3. The thick arrow indicates a region of enhancing tumor margin; the thin arrow in B indicates edematous brain. A, Contrast-enhanced T1-weighted volume image. B, T2-weighted EP images. C, 〈D〉 parametric map. Note the diffuse nature of the edema. D, FA parametric map.
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