期刊
RADIOGRAPHICS
卷 29, 期 6, 页码 1653-U142出版社
RADIOLOGICAL SOC NORTH AMERICA
DOI: 10.1148/rg.296095520
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资金
- NIDDK NIH HHS [R01 DK074718] Funding Source: Medline
Magnetic resonance (MR) spectroscopy allows the demonstration of relative tissue metabolite concentrations along a two- or three-dimensional spectrum based on the chemical shift phenomenon. An MR spectrum is a plot of the signal intensity and frequency of a chemical or metabolite within a given voxel. At proton MR spectroscopy, the frequency at which a chemical or compound occurs depends on the configuration of the protons within the structure of that chemical. At in vivo proton MR spectroscopy, the frequency location of water is used as the standard of reference to identify a chemical. The frequency shift or location of chemicals relative to that of water allows generation of qualitative and quantitative information about the chemicals that occur within tissues, forming the basis of tissue characterization by MR spectroscopy. MR spectroscopy also may be used to quantify liver fat by measuring lipid peaks and to diagnose malignancy, usually by measuring the choline peak. Interpretation of MR spectroscopic data requires specialized postprocessing software and is subject to technical limitations including low signal-to-noise ratio, masking of metabolite peaks by dominant water and lipid peaks, partial-volume averaging from other tissue within the voxel, and phase and frequency shifts from motion. MR spectroscopy of the liver is an evolving technology with potential for improving the diagnostic accuracy of tissue characterization when spectra are interpreted in conjunction with MR images. (C) RSNA, 2009 . radiographics.rsna.org
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