Fast T2-weighted MRI of the prostate at 3 tesla
Purpose: To describe a rapid T2*‐weighted (T2*W), three‐dimensional (3D) echo planar imaging (EPI) sequence and its application in mapping local magnetic susceptibility variations in 3 Tesla (T) prostate MRI. To compare the sensitivity of T2*W EPI with routinely used T1‐weighted turbo‐spin echo sequ...
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Veröffentlicht in: | Journal of magnetic resonance imaging 2011-04, Vol.33 (4), p.902-907 |
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Sprache: | eng |
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Zusammenfassung: | Purpose:
To describe a rapid T2*‐weighted (T2*W), three‐dimensional (3D) echo planar imaging (EPI) sequence and its application in mapping local magnetic susceptibility variations in 3 Tesla (T) prostate MRI. To compare the sensitivity of T2*W EPI with routinely used T1‐weighted turbo‐spin echo sequence (T1W TSE) in detecting hemorrhage and the implications on sequences sensitive to field inhomogeneities such as MR spectroscopy (MRS).
Materials and Methods:
B0 susceptibility weighted mapping was performed using a 3D EPI sequence featuring a 2D spatial excitation pulse with gradients of spiral k‐space trajectory. A series of 11 subjects were imaged using 3T MRI and combination endorectal (ER) and six‐channel phased array cardiac coils. T1W TSE and T2*W EPI sequences were analyzed quantitatively for hemorrhage contrast. Point resolved spectroscopy (PRESS MRS) was performed and data quality was analyzed.
Results:
Two types of susceptibility variation were identified: hemorrhagic and nonhemorrhagic T2*W‐positive areas. Post‐biopsy hemorrhage lesions showed on average five times greater contrast on the T2*W images than T1W TSE images. Six nonhemorrhage regions of severe susceptibility artifact were apparent on the T2*W images that were not seen on standard T1W or T2W images. All nonhemorrhagic susceptibility artifact regions demonstrated compromised spectral quality on 3D MRS.
Conclusion:
The fast T2*W EPI sequence identifies hemorrhagic and nonhemorrhagic areas of susceptibility variation that may be helpful in prostate MRI planning at 3.0T. J. Magn. Reson. Imaging 2011;33:902–907. © 2011 Wiley‐Liss, Inc. |
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ISSN: | 1053-1807 1522-2586 |
DOI: | 10.1002/jmri.22496 |