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. 2011 Mar 29;11(1):31–36. doi: 10.1102/1470-7330.2011.0007

Table 1.

MRI parameters used in the current study

MRI sequence TR/TE (ms) FOV (mm) Resolution (mm) Matrix Flip angle Slice thickness (mm)
Sagittal T2W TSE 2659/120 140 0.46 × 0.6 × 3.0 304× 234 90 3
Axial T2W TSE 4434/120 140 0.46 × 0.6 × 3.0 304× 234 90 3
Coronal T2W TSE 2174/120 140 0.46 × 0.6 × 3.0 304× 234 90 3
Axial DW MRIa 5770/52 160 1.25 × 1.25 × 3.0 112× 108 90 3
3D MR PRESSb 980/100 72 6.0 × 6.0 × 6.0 10× 10 90 6
Axial pre-contrast T1 5.5/2.1 260 0.86 × 1.18 × 6.0 256× 186 5 6
Axial 3D DCEc 5.5/2.1 260 0.86 × 1.18 × 6.0 188× 96 15 6

FOV, field of view; TE, echo time; TR, repetition time; TSE, turbo spin echo.

aAxial DW multi-slice images with 20 slices taken with 5 evenly spaced B values from 0 to 750 s/mm2 and ADC maps were calculated.

b3D MR point resolved spectroscopy; water and fat signals were suppressed before data collection; each spectrum (1024 complex points) was obtained from a voxel size of 6 × 6 × 6 mm3 tissue with spectral width of 2000 Hz. Second-order shimming was used to maximize magnetic field homogeneity in the localized volume.

cAxial DCE images before, during, and after a single-dose injection of gadopentetate dimeglumine (Magnevist, Berlex, Wayne, NJ, USA) at a dose of 0.1 mmol/kg through a peripheral vein at a rate of 3 ml/s via a mechanical injector (Spectris MR Injection System, Medrad, Pittsburgh, PA, USA). The DCE acquisition consisted of a 10-slice, 3D T1W fast-field echo with a phase encoding direction from left to right without fat saturation. Four unenhanced sets (13 s) and approximately 96 contrast-enhanced sets of images were acquired sequentially without a delay between acquisitions. A total of 1000 images were obtained during DCE MRI (temporal resolution = 3.1 s).