Rinsho Shinkeigaku
Online ISSN : 1882-0654
Print ISSN : 0009-918X
ISSN-L : 0009-918X
Case Reports
Diagnosis of pediatric multiple sclerosis initially presenting with tumefactive demyelinating lesion using 1H-magnetic resonance spectroscopy
Takashi KageyamaYoko GotohFumie SanoTakeo KatohMituhiko NambuTsutomu OkadaToshihiko Suenaga
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JOURNAL FREE ACCESS

2011 Volume 51 Issue 9 Pages 688-693

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Abstract

We report a case of tumefactive demyelinating lesion (TDL) diagnosed using 1H-magnetic resonance spectroscopy (1H-MRS) and conventional magnetic resonance imaging (MRI). A 7-year-old girl was admitted to our hospital with complaints of sleepiness and clumsiness of the right limbs. Neurological examination showed somnolence, right-sided apraxia, and hemiparesis with enhanced tendon reflexes and Babinski sign. Conventional brain MRI revealed extensive hyperintensity in the subcortical white matter of the left frontal lobe in both T2 weighted and fluid attenuated inversion recovery images. Gadolinium-enhanced T1 weighted images showed a tumor-like lesion in this area with interrupted rim enhancement, termed open ring sign, and a periventricular lesion along the inferior horn of the right lateral ventricle and a juxtacortical lesion under the right motor cortex. In 1H-MRS, both single voxel spectroscopy (SVS) and chemical shift imaging showed elevation of choline and reduction of N-acetylaspartate in the left frontal lobe lesion. Furthermore, SVS with a short echo time revealed elevated peaks for glutamate/glutamine complex in this lesion. These results suggested the demyelinating nature of this tumor-like lesion, in accordance with the concept of TDL. Based on this diagnosis, we treated the patient with three sets of methylprednisolone pulse therapy, which resulted in the reduction of TDL and neurological improvement. A follow-up study using MRI also demonstrated two more lesions in the corona radiata and internal capsule of the left hemisphere, supporting a diagnosis of multiple sclerosis based on the revised McDonald's criteria (2010). We concluded that 1H-MRS may be beneficial in the differential diagnosis of TDL.

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© 2011 Societas Neurologica Japonica
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