Criteria for early detection of conduction block in multifocal motor neuropathy (MMN): a study based on control populations and follow-up of MMN patients

被引:33
作者
Cappellari, A [1 ]
NobileOrazio, E [1 ]
Meucci, N [1 ]
Minzi, GL [1 ]
Scarlato, G [1 ]
Barbieri, S [1 ]
机构
[1] UNIV MILAN,IRCCS,OSPED MAGGIORE POLICLIN,INST CLIN NEUROL,I-20122 MILAN,ITALY
关键词
multifocal motor neuropathy; amyotrophic lateral sclerosis; electrophysiological follow-up; conduction block; diagnostic criteria;
D O I
10.1007/s004150050157
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Motor conduction block (MCB) has been used as the main diagnostic criterion in multifocal motor neuropathy (MMN). Nonetheless, no agreed definition of block currently exists; the proposed required percent decrement of proximal compound muscle action potential (CMAP) amplitude varies from > 20% to > 50%. The aim of this work was to-evaluate, through a follow-up study of patients with MMN, the behaviour of MCB over time. The percent decrement and temporal dispersion of proximal CMAP have also been calculated in normal controls and in patients affected by amyotrophic lateral sclerosis (ALS). The results show that MCB in patients with MMN is a dynamic entity which greatly varies over time and that a > 50% CMAP amplitued reduction may well be preceded by a smaller decrement that is nonetheless indicative of focal myelin damage in the appropriate clinical context. This datum and the results obtained in the control group and in patients with ALS suggest that a reappraisal of the diagnostic criteria for MCB, in cases with clinical and electrophysiological data strongly indicative of MMN, should be considered. Since MMN is a treatable disorder, the use of the proposed less restrictive criteria for the identification of MCB could allow for a promp and more effective treatment.
引用
收藏
页码:625 / 630
页数:6
相关论文
共 25 条
[1]   ROLE OF ELECTROMYOGRAPHY IN AMYOTROPHIC-LATERAL-SCLEROSIS [J].
BEHNIA, M ;
KELLY, JJ .
MUSCLE & NERVE, 1991, 14 (12) :1236-1241
[2]   CONDUCTION BLOCK AND DENERVATION IN GUILLAIN-BARRE POLYNEUROPATHY [J].
BROWN, WF ;
FEASBY, TE .
BRAIN, 1984, 107 (MAR) :219-239
[3]  
Cappellari A, 1996, MUSCLE NERVE, V19, P666, DOI 10.1002/(SICI)1097-4598(199605)19:5<666::AID-MUS19>3.0.CO
[4]  
2-L
[5]   MULTIFOCAL MOTOR NEUROPATHY - ELECTRODIAGNOSTIC FEATURES [J].
CHAUDHRY, V ;
CORSE, AM ;
CORNBLATH, DR ;
KUNCL, RW ;
FREIMER, ML ;
GRIFFIN, JW .
MUSCLE & NERVE, 1994, 17 (02) :198-205
[6]   MULTIFOCAL MOTOR NEUROPATHY - RESPONSE TO HUMAN IMMUNE GLOBULIN [J].
CHAUDHRY, V ;
CORSE, AM ;
CORNBLATH, DR ;
KUNCL, RW ;
DRACHMAN, DB ;
FREIMER, ML ;
MILLER, RG ;
GRIFFIN, JW .
ANNALS OF NEUROLOGY, 1993, 33 (03) :237-242
[7]   IMMUNOSUPPRESSIVE TREATMENT IN MULTIFOCAL MOTOR NEUROPATHY [J].
FELDMAN, EL ;
BROMBERG, MB ;
ALBERS, JW ;
PESTRONK, A .
ANNALS OF NEUROLOGY, 1991, 30 (03) :397-401
[8]   MULTIFOCAL DEMYELINATING MOTOR NEUROPATHY - CRANIAL NERVE INVOLVEMENT AND IMMUNOGLOBULIN THERAPY [J].
KAJI, R ;
SHIBASAKI, H ;
KIMURA, J .
NEUROLOGY, 1992, 42 (03) :506-509
[9]   A SYNDROME OF ASYMMETRIC LIMB WEAKNESS WITH MOTOR CONDUCTION BLOCK [J].
KRARUP, C ;
STEWART, JD ;
SUMNER, AJ ;
PESTRONK, A ;
LIPTON, SA .
NEUROLOGY, 1990, 40 (01) :118-127
[10]  
KUNTZER T, 1995, REV NEUROL-FRANCE, V151, P368