Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature review

被引:6
作者
Alboini, Paolo Emilio [1 ]
Damato, Valentina [1 ]
Iorio, Raffaele [2 ]
Luigetti, Marco [1 ]
Evoli, Amelia [1 ]
机构
[1] Univ Cattolica Sacro Cuore, Inst Neurol, I-00168 Rome, Italy
[2] Don Carlo Gnocchi ONLUS Fdn, Milan, Italy
关键词
Myasthcnia gravis; Lambert-Eaton myasthenic syndrome; Presynaptic neurophysiological pattern; Cholinesterase inhibitors; 3,4-Diaminopyridine; EATON-LAMBERT SYNDROME; NEUROMUSCULAR-TRANSMISSION; IMMUNOLOGICAL EVIDENCE; PATIENT; FEATURES; WEAKNESS; MG;
D O I
10.1016/j.nmd.2015.04.012
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The distinction between myasthenia gravis and Lambert Eaton myasthenic syndrome is based on clinical, neurophysiological and immunological features. We hereby report two cases with a clinical diagnosis of myasthenia gravis and neurophysiological features consistent with a pre-synaptic neuromuscular transmission defect. Both patients had increased anti-acetylcholine receptor antibody titres and showed a good response to cholinesterase inhibitors, along with a >100% facilitation of the compound muscle action potential on electrophysiological studies. We provide a review of English literature studies on co-existing features of myasthenia gravis and Lambert Eaton myasthenic syndrome, and discuss diagnostic controversies. (C) 2015 Elsevier By. All rights reserved.
引用
收藏
页码:646 / 650
页数:5
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