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British Journal of Radiology (2003) 76, 459-463
© 2003 British Institute of Radiology
doi: 10.1259/bjr/16316438

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Could assessment of glioma methylene lipid resonance by in vivo 1H-MRS be of clinical value?

P S Murphy, PhD1, I J Rowland, PhD1, L Viviers, MBChB2, M Brada, BSc, FRCP, FRCR2, M O Leach, PhD, FinstP, FMedSci1 and A S K Dzik-Jurasz, PhD, FRCS, FRCR1

1 Cancer Research UK Clinical MR Research Group and 2 Department of Neuro-oncology, The Institute of Cancer Research and The Royal Marsden NHS Trust, Sutton, Surrey SM2 5PT, UK



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Figure 1. (a) A short echo time spectrum from a low grade tumour showing no contrast enhancement as evidenced by imaging and water 1H-MRS. The major resonances are indicated: Cho, choline; Cre, creatine; and NAA, N-acetylaspartate. (b). A short echo time spectrum from a histologically verified contrast enhancing high grade glioma. The most prominent peaks observed are the lipid methylene and methyl signals, labelled as lip(-CH2-) and lip(-CH3), respectively.

 


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Figure 2. (a) The relationship between glioma grade and the normalized lipid methylene signal. (b) The intravoxel enhancement (IVE) values determined spectroscopically and categorized by tumour grade.

 


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Figure 3. A correlation between the normalized lipid methylene signal with the percentage intravoxel enhancement (IVE). For the linear regression, r2=0.74 and p=0.0002.

 





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