Neuroimaging in amyotrophic lateral sclerosis

被引:37
作者
Comi, G [1 ]
Rovaris, M [1 ]
Leocani, L [1 ]
机构
[1] Osped San Raffaele, Inst Sci, Dept Neurophysiol, I-20132 Milan, Italy
关键词
amyotrophic lateral sclerosis; magnetic resonance spectroscopy; magnetization transfer imaging; diffusion weighted imaging;
D O I
10.1046/j.1468-1331.1999.660629.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Amyotrophic lateral sclerosis (ALS) is a chronic degenerative disorder of unknown etiology affecting the motor system. Conventional and non-conventional neuroimaging techniques can provide essential help both to increase the confidence in ALS diagnosis and to assess the disease evolution. Signal abnormalities at the level of the motor cortex and the corticospinal tract on conventional T2-weighted magnetic resonance (MR) images are a potentially useful marker of ALS pathology. However, the prognostic value of these conventional MR abnormalities is still hampered by their low pathological specificity. Non-conventional MR techniques with a higher pathological specificity, such as MR spectroscopy, magnetization transfer imaging and diffusion-weighted imaging, seem to have some potential not only for ALS diagnosis, but also for monitoring disease evolution either naturally or when modified by experimental treatments. Eur J Neurol 6:629-637 (C) 1999 Lippincott Williams & Wilkins.
引用
收藏
页码:629 / 637
页数:9
相关论文
共 56 条
[1]   REDUCED ISOTOPE UPTAKE RESTRICTED TO THE MOTOR AREA IN PATIENTS WITH AMYOTROPHIC-LATERAL-SCLEROSIS [J].
ABE, K ;
YORIFUJI, S ;
NISHIKAWA, Y .
NEURORADIOLOGY, 1993, 35 (06) :410-411
[2]   Cognitive function in amyotrophic lateral sclerosis [J].
Abe, K ;
Fujimura, H ;
Toyooka, K ;
Sakoda, S ;
Yorifuji, S ;
Yanagihara, T .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1997, 148 (01) :95-100
[3]   Frontal lobe dysfunction in amyotrophic lateral sclerosis - A PET study [J].
Abrahams, S ;
Goldstein, LH ;
Kew, JJM ;
Brooks, DJ ;
Lloyd, CM ;
Frith, CD ;
Leigh, PN .
BRAIN, 1996, 119 :2105-2120
[4]   Proton magnetic resonance spectroscopy of the primary motor cortex in patients with motor neuron disease -: Subgroup analysis and follow-up measurements [J].
Block, W ;
Karitzky, J ;
Träber, F ;
Pohl, C ;
Keller, E ;
Mundegar, RR ;
Lamerichs, R ;
Rink, H ;
Ries, F ;
Schild, HH ;
Jerusalem, F .
ARCHIVES OF NEUROLOGY, 1998, 55 (07) :931-936
[6]  
BROWNELL B, 1970, J NEUROL NEUROSUR PS, V33, P388
[7]  
Charcot J, 1869, Arch Physiol Neurol Pathol, V2, P744
[8]   AMYOTROPHIC-LATERAL-SCLEROSIS - CORRELATION OF CLINICAL AND MR-IMAGING FINDINGS [J].
CHEUNG, G ;
GAWAL, MJ ;
COOPER, PW ;
FARB, RI ;
ANG, LC .
RADIOLOGY, 1995, 194 (01) :263-270
[9]   LOWERED CEREBRAL GLUCOSE-UTILIZATION IN AMYOTROPHIC-LATERAL-SCLEROSIS [J].
DALAKAS, MC ;
HATAZAWA, J ;
BROOKS, RA ;
DICHIRO, G .
ANNALS OF NEUROLOGY, 1987, 22 (05) :580-586
[10]   Amyotrophic lateral sclerosis - Origin and extent of the upper motor neuron lesion [J].
Davison, C .
ARCHIVES OF NEUROLOGY AND PSYCHIATRY, 1941, 46 (06) :1039-1056