Demyelinating lesions in the cervical cord in multiple sclerosis 10 years after onset of the disease. Correlation between MRI parameters and clinical course

被引:0
作者
Bonek, Robert [1 ]
Orlicka, Katarzyna [2 ]
Maciejek, Zdzislaw [1 ]
机构
[1] Wojskowy Szpital Kliniczny Poliklin Bydgoszczy, Neurol Klin 10, Warsaw, Poland
[2] Wojskowy Szpital Kliniczny Poliklin Bydgoszczy, Zaklad Radiol 10, Warsaw, Poland
关键词
multiple sclerosis; cervical cord MRI; demyelinating lesions; cord atrophy; SPINAL-CORD; ABNORMALITIES; DISABILITY; BRAIN; MS;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and purpose: Demyelinating lesions in spinal cord in multiple sclerosis (MS) are found in magnetic resonance imaging (MRI) in 47-90% of patients; spinal cord atrophy, however, which is a measure of axonal loss and correlates with disability, is found in 13-41% of patients. Presence and character of lesions depend on the duration and progression of the disease. The aim of this study was to estimate the presence, character and location of lesions and cervical cord atrophy in MRI performed 10 years after the onset of MS in relation to the clinical course. Material and methods: 60 patients (41 females and 19 males) with definite MS according to McDonald's criteria were studied. The age of patients ranged from 29 to 62 years and disease duration ranged from I I to 40 years. The MS group comprised 20 patients with secondary progressive MS (SPMS), 20 patients with primary progressive MS (PPMS) and 20 patients with benign form of MS (BMS). Spinal cord MRI was performed in conventional T1 and T2-weighted sequences. Results: Demyelinating lesions were found in 62% of patients (50916 of patients with BMS, 60% with PPMS and 75% with SPMS). 42 intrinsic focal lesions were identified in 18 patients and diffuse lesions of spinal cord were noted in 19 patients. Focal lesions were seen in patients with BMS, whereas SPMS patients had diffuse cervical cord abnormalities, and PPMS patients exhibited both forms of changes. 60% of intrinsic focal lesions were located at C3-C5 levels. Medium-sized lesions prevailed in BMS form; in PPMS form small and medium-size lesions, and in SPMS form large lesions (>10 mm) were more frequent. The spinal cord was atrophic in 8% of patients (10% of patients with PPMS and 15% with SPMS). In BMS no atrophy of the cervical cord was observed. We did not find focal demyelinating lesions in the cervical segment of patients with spinal cord atrophy. Conclusions: Presence and character of demyelinating lesions in cervical cord ten years after onset of MS is significantly related to the clinical form of the disease. The mid-cervical region of the spinal cord appeared to be the commonest location of the focal lesions. Cervical cord atrophy was more frequent in patients with PPMS and SPMS, but it was not accompanied with intrinsic focal cord lesions.
引用
收藏
页码:229 / 233
页数:5
相关论文
共 12 条
[1]  
Bonek Robert, 2004, Neurol Neurochir Pol, V38, P25
[2]   Spinal cord abnormalities in recently diagnosed MS patients [J].
Bot, JCJ ;
Barkhof, F ;
Polman, CH ;
Nijeholt, GJLA ;
de Groot, V ;
Bergers, E ;
Ader, HJ ;
Castelijns, JA .
NEUROLOGY, 2004, 62 (02) :226-233
[3]   Multiple sclerosis [J].
Compston, A ;
Coles, A .
LANCET, 2002, 359 (9313) :1221-1231
[4]   A spinal cord MRI study of benign and secondary progressive multiple sclerosis [J].
Filippi, M ;
Campi, A ;
Colombo, B ;
Pereira, C ;
Martinelli, V ;
Baratti, C ;
Comi, G .
JOURNAL OF NEUROLOGY, 1996, 243 (07) :502-505
[5]   A conventional and magnetization transfer MRI study of the cervical cord in patients with MS [J].
Filippi, M ;
Bozzali, M ;
Horsfield, MA ;
Rocca, MA ;
Sormani, MP ;
Iannucci, G ;
Colombo, B ;
Comi, G .
NEUROLOGY, 2000, 54 (01) :207-213
[6]   SPINAL-CORD MRI USING MULTIARRAY COILS AND FAST SPIN-ECHO .2. FINDINGS IN MULTIPLE-SCLEROSIS [J].
KIDD, D ;
THORPE, JW ;
THOMPSON, AJ ;
KENDALL, BE ;
MOSELEY, IF ;
MACMANUS, DG ;
MCDONALD, WI ;
MILLER, DH .
NEUROLOGY, 1993, 43 (12) :2632-2637
[7]  
KURTZKE JF, 1983, NEUROLOGY, V33, P1444, DOI 10.1212/WNL.33.11.1444
[8]   Spinal cord atrophy and disability in multiple sclerosis - A new reproducible and sensitive MRI method with potential to monitor disease progression [J].
Losseff, NA ;
Webb, SL ;
ORiordan, JI ;
Page, R ;
Wang, L ;
Barker, GJ ;
Tofts, PS ;
McDonald, WI ;
Miller, DH ;
Thompson, AJ .
BRAIN, 1996, 119 :701-708
[9]   Recommended diagnostic criteria for multiple sclerosis: Guidelines from the International Panel on the Diagnosis of Multiple Sclerosis [J].
McDonald, WI ;
Compston, A ;
Edan, G ;
Goodkin, D ;
Hartung, HP ;
Lublin, FD ;
McFarland, HF ;
Paty, DW ;
Polman, CH ;
Reingold, SC ;
Sandberg-Wollheim, M ;
Sibley, W ;
Thompson, AJ ;
van den Noort, S ;
Weinshenker, BY ;
Wolinsky, JS .
ANNALS OF NEUROLOGY, 2001, 50 (01) :121-127
[10]   Brain and spinal cord abnormalities in multiple sclerosis - Correlation between MRI parameters, clinical subtypes and symptoms [J].
Nijeholt, GJLA ;
van Walderveen, MAA ;
Castelijns, JA ;
van Waesberghe, JHTM ;
Polman, C ;
Scheltens, P ;
Rosier, PFWM ;
Jongen, PJH ;
Barkhof, F .
BRAIN, 1998, 121 :687-697