Severe metabolic abnormalities in the white matter of patients with vacuolating megalencephalic leukoencephalopathy with subcortical cysts. A proton MR spectroscopic imaging study

被引:34
作者
De Stefano, N
Balestri, P
Dotti, MT
Grosso, S
Mortilla, M
Morgese, G
Federico, A
机构
[1] Univ Siena, Inst Pediat Clin, I-53100 Siena, Italy
[2] Univ Siena, NMR Ctr, I-53100 Siena, Italy
[3] Univ Siena, Ctr Diag Prevent & Therapy Neurol Handicaps, I-53100 Siena, Italy
关键词
megalencephaly; cysts; leukoencephalopathy; white matter; magnetic resonance spectroscopy;
D O I
10.1007/s004150170182
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Vacuolating megalencephalic leukoencephalopathy (VML) with subcortical cysts is a neurodegenerative disorder clinically characterized by megalencephaly with onset in the first year of life, progressive ataxia, spasticity and relatively spared cognitive function. Conventional MRI findings consist of diffusely abnormal cerebral white matter with subcortical cysts. Recent single-voxel proton MR spectroscopy studies have shown mild metabolic abnormalities in the white matter. We report here a combined proton MR imaging and MR spectroscopic imaging (H-1-MRSI) study on new, unrelated patients with this rare disorder. H-1-MRSI examinations, which can provide simultaneously metabolic information from many different brain regions, showed inhomogeneous decreases in all normally detected metabolites with significant widespread decreases in the ratio of N-acetylaspartate to creatine+phosphocreatine and concomitant small increases in lactate in the white matter of both hemispheres. Metabolic abnormalities were milder in the frontal white matter and more severe in the posterior white matter. The H-1-MRSI pattern of the gray matter was normal in both patients. In one patient, a subsequent H-1-MRSI examination (performed 3 years after the first) confirmed the presence of widespread decreases in the ratio of N-acetylaspartate to creatine+phosphocreatine in the white matter. We conclude that severe metabolic abnormalities can be found in the white matter of VML patients. This suggests that, despite the apparently mild clinical course, a severe neurodegenerative process may occur in the white matter of these patients.
引用
收藏
页码:403 / 409
页数:7
相关论文
共 31 条
[1]  
Arnold DL, 1996, MR SPECTROSCOPY CLIN, P139
[2]   L-2-HYDROXYGLUTARIC ACIDEMIA - A NOVEL INHERITED NEUROMETABOLIC DISEASE [J].
BARTH, PG ;
HOFFMANN, GF ;
JAEKEN, J ;
LEHNERT, W ;
HANEFELD, F ;
VANGENNIP, AH ;
DURAN, M ;
VALK, J ;
SCHUTGENS, RBH ;
TREFZ, FK ;
REIMANN, G ;
HARTUNG, HP .
ANNALS OF NEUROLOGY, 1992, 32 (01) :66-71
[3]   In vitro expression of N-acetyl aspartate by oligodendrocytes:: Implications for proton magnetic resonance spectroscopy signal in vivo [J].
Bhakoo, KK ;
Pearce, D .
JOURNAL OF NEUROCHEMISTRY, 2000, 74 (01) :254-262
[4]   APPLICATION OF TIME-DOMAIN FITTING IN THE QUANTIFICATION OF INVIVO H-1 SPECTROSCOPIC IMAGING DATA SETS [J].
DEBEER, R ;
VANDENBOOGAART, A ;
VANORMONDT, D ;
PIJNAPPEL, WWF ;
DENHOLLANDER, JA ;
MARIEN, AJH ;
LUYTEN, PR .
NMR IN BIOMEDICINE, 1992, 5 (04) :171-178
[5]  
DENHOLLANDER JA, 1991, P SOC MAGN RESON MED, V1, P472
[6]  
DESTEFANO N, 1995, MAGN RESON MED, V34, P721
[7]   Chemical pathology of acute demyelinating lesions and its correlation with disability [J].
DeStefano, N ;
Matthews, PM ;
Antel, JP ;
Preul, M ;
Francis, G ;
Arnold, DL .
ANNALS OF NEUROLOGY, 1995, 38 (06) :901-909
[8]  
Dubeau F, 2000, ANN NEUROL, V47, P179, DOI 10.1002/1531-8249(200002)47:2<179::AID-ANA7>3.0.CO
[9]  
2-Z
[10]   SPONGY DEGENERATION OF THE NEURAXIS (CANAVAN VAN BOGAERT DISEASE) AND N-ACETYLASPARTIC ACIDURIA [J].
ECHENNE, B ;
DIVRY, P ;
VIANEYLIAUD, C .
NEUROPEDIATRICS, 1989, 20 (02) :79-81