Structural and Metabolic Features of Two Different Variants of Multiple Sclerosis: A PET/MRI Study

被引:25
作者
Bolcaen, Julie [1 ]
Acou, Marjan [2 ]
Mertens, Koen [1 ]
Hallaert, Giorgio [3 ]
Van den Broecke, Caroline [4 ]
Achten, Eric [2 ]
Goethals, Ingeborg [1 ]
机构
[1] Ghent Univ Hosp, Dept Nucl Med, B-9000 Ghent, Belgium
[2] Ghent Univ Hosp, Dept Radiol, B-9000 Ghent, Belgium
[3] Ghent Univ Hosp, Dept Neurosurg, B-9000 Ghent, Belgium
[4] Ghent Univ Hosp, Dept Pathol, B-9000 Ghent, Belgium
关键词
Multiple sclerosis; MRI; MR spectroscopy; PET; F-18; fluoromethylcholine; fluorodeoxyglucose; POSITRON-EMISSION-TOMOGRAPHY; PROTON MR SPECTROSCOPY; TUMOR;
D O I
10.1111/j.1552-6569.2012.00760.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND Multimodality imaging such as proton magnetic resonance spectroscopy (MRS) and positron emission tomography (PET) have provided information specific to the underlying mechanisms of many brain diseases, including multiple sclerosis (MS). PURPOSE To determine the structural and metabolic characterization of two particular variants of MS, namely tumefactive MS and Balo's concentric sclerosis (BCS). METHODS Conventional MR imaging, diffusion and perfusion MR, MR spectroscopy and PET imaging with F-18 fluorodeoxyglucose (FDG) and F-18 fluoromethylcholine (FCho) were performed. RESULTS In a case with pathologically proven tumefactive MS, magnetic resonance imaging (MRI) showed a pseudotumoral lesion with incomplete ring enhancement, peripheral diffusion restriction, and high choline and lactate peaks on MRS. On follow-up, the lesion showed significant growth. In a case of BCS, MRI showed an onion-like lesion without contrast enhancement or diffusion restriction, and only a moderate increase in choline on MRS. The lesion remained stable on follow-up. On PET, there was no uptake of F-18 FDG in either type of MS lesion. Conversely, uptake of F-18 FCho was moderate in tumefactive MS, whereas no F-18 FCho uptake was noted in the lesion with, on MRI, typical features of BCS. CONCLUSIONS Our findings illustrate that metabolic features may differ between variants of MS possibly signifying different disease activity.
引用
收藏
页码:431 / 436
页数:6
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