Genovese O, Ballario C, Storino R, Segura E, Sica R E
Division Neurologia, Universidad de Buenos Aires.
Arq Neuropsiquiatr. 1996 Jun;54(2):190-6. doi: 10.1590/s0004-282x1996000200002.
We conducted a clinical and electromyographical study in patients with Chagas' disease in the indeterminate or chronic stages of the illness. Altogether 841 patients were examined. Only 511 were admitted within the protocol; the remainder patients were rejected because they showed other causes able to damage the nervous system. Fifty two (10.17%) out of the 511 patients showed signs and symptoms of peripheral nervous system involvement in the form of sensory impairment and diminished tendon jerks suggesting the presence of neuropathy. Forty five of them were submitted to a conventional electromyographical examination. Fifteen of them showed normal results, while the remainder 30 disclosed a reduced interference pattern, being most of the remaining motor unit potentials fragmented or poliphasic, reduced sensory and motor conduction velocities and diminished amplitude of the sensory action potential. The findings suggest that some chagasic patients in the indeterminate or chronic stages of the disease may develop a clinical mild sensory-motor peripheral neuropathy.
我们对处于恰加斯病不确定期或慢性期的患者进行了一项临床和肌电图研究。总共检查了841名患者。只有511名患者符合方案纳入标准;其余患者因显示出其他能够损害神经系统的病因被排除。511名患者中有52名(10.17%)表现出外周神经系统受累的体征和症状,形式为感觉障碍和腱反射减弱,提示存在神经病变。其中45名患者接受了传统肌电图检查。15名结果正常,其余30名显示干扰图形减少,其余大多数运动单位电位呈多相或碎片化,感觉和运动传导速度降低,感觉动作电位幅度减小。这些发现表明,一些处于恰加斯病不确定期或慢性期的患者可能会发展为临床症状轻微的感觉运动性外周神经病变。