Garcia Erro M I, Sica R E, Losavio A S, Muchnik S, Arroyo H
Sección Electroneurofisiología Clinica, Div. Neurología, Urquiza Bs, As., Argentina.
Neuropediatrics. 1988 May;19(2):92-5. doi: 10.1055/s-2008-1052408.
Twelve patients between 15 months and 13 years of age with clinical and pharmacological features of myasthenia gravis were studied. Repetitive nerve stimulation did not offer valuable information; the patients demonstrated either inspecific muscular decremental response or had normal behavior. Two clear groups of patients were identified after measurements of acetylcholine receptor (AChR) antibodies and MEPP amplitude recorded in the diaphragm of mice injected with sera from those patients. The first group included patients with positive AChR antibodies titers and decreased MEPP amplitude. The second one had negative AChR antibodies titers and MEPPs with normal amplitude. These data strongly suggest immunologic and non-immunologic mechanisms for the former and later respectively.
对12名年龄在15个月至13岁之间具有重症肌无力临床和药理学特征的患者进行了研究。重复神经刺激未提供有价值的信息;这些患者要么表现出非特异性肌肉递减反应,要么行为正常。在测量注射这些患者血清的小鼠膈肌中的乙酰胆碱受体(AChR)抗体和微小终板电位(MEPP)幅度后,确定了两组明显不同的患者。第一组患者的AChR抗体滴度呈阳性且MEPP幅度降低。第二组患者的AChR抗体滴度呈阴性且MEPP幅度正常。这些数据有力地分别提示了前者的免疫机制和后者的非免疫机制。