Tsujihata M, Yoshimura T, Satoh A, Kinoshita I, Matsuo H, Mori M, Nagataki S
School of Allied Sciences, Nagasaki University, Japan.
Neurology. 1989 Oct;39(10):1359-63. doi: 10.1212/wnl.39.10.1359.
We detected deposits of IgG, C3, and C9 (immune complexes) at the limb muscle motor end-plates (biceps brachii muscle) in 16 of 19 patients who exhibited only ocular signs and symptoms of myasthenia gravis that were improved by intravenous injections of edrophonium chloride. Circulating anti-acetylcholine receptor (anti-AChR) antibodies were negative in 6 of the 16 patients, but the motor end-plate fine structure in the postsynaptic regions was abnormal in all 16. Single-fiber EMG revealed no abnormalities in 8 of 13 patients studied. Our results indicate that the detection of immune complexes at the limb muscle end-plate provides a highly sensitive and confirmative method for diagnosing patients with minimal or atypical myasthenia gravis who have no detectable anti-AChR antibodies in their serum.
在19例仅表现为重症肌无力眼部症状和体征且静脉注射氯化腾喜龙后症状改善的患者中,我们在16例患者的肢体肌肉运动终板(肱二头肌)处检测到IgG、C3和C9沉积物(免疫复合物)。16例患者中有6例循环抗乙酰胆碱受体(抗AChR)抗体呈阴性,但所有16例患者突触后区域的运动终板精细结构均异常。单纤维肌电图显示,在接受研究的13例患者中,8例没有异常。我们的结果表明,在肢体肌肉终板处检测免疫复合物为诊断血清中无可检测到抗AChR抗体的轻症或非典型重症肌无力患者提供了一种高度敏感且具有确诊意义的方法。