首页> 外文OA文献 >An Experience of Electrophysiological Studies on a Patient With Anti-MuSK and Anti-acetylcholine Receptor Antibody Negative Myasthenia Gravis(Special Issue in Hornor of the Retirement of Professor Makoto Iwata at the Department of Neurology, Tokyo Womenu27s Medical University)
【2h】

An Experience of Electrophysiological Studies on a Patient With Anti-MuSK and Anti-acetylcholine Receptor Antibody Negative Myasthenia Gravis(Special Issue in Hornor of the Retirement of Professor Makoto Iwata at the Department of Neurology, Tokyo Womenu27s Medical University)

机译:抗MuSK和抗乙酰胆碱受体抗体阴性重症肌无力患者的电生理研究经验(东京女子医科大学神经病学系岩田诚教授退休的角质特刊)

摘要

We encountered an acetylcholine receptor (AChR) and muscle-specific tyrosine kinase (MuSK) antibody-negative myasthenia gravis (MG) patient with unique semiological and electrophysiological features. MG patients are divided into those with positive and negative anti-AChR antibody. It is occasionally difficult to diagnose as MG in patients with negative anti-AChR antibody. Because in our patient both anti-AChR and MuSK antibodies were negative, we had great difficulty in making definite diagnosis of MG. However, we were able to diagnose our patient as MG using combined edrophonium test and electrophysiological study. This combination may have a possibility to be applied in similar cases like ours. In addition, it was suggested from unique semiological and electrophysiological features that our patient had different pathogenesis from usual MG patients.
机译:我们遇到了具有独特的符号学和电生理学特征的乙酰胆碱受体(AChR)和肌肉特异性酪氨酸激酶(MuSK)抗体阴性重症肌无力(MG)患者。 MG患者分为抗AChR抗体阳性和阴性的患者。抗AChR抗体阴性的患者有时很难诊断为MG。因为在我们的患者中,抗AChR和MuSK抗体均为阴性,所以我们很难对MG进行明确诊断。但是,我们可以通过结合使用edrophonium测试和电生理研究来将我们的患者诊断为MG。这种组合可能有可能在类似我们的类似情况下应用。另外,从独特的符号学和电生理学特征表明,我们的患者与普通的MG患者有不同的发病机理。

著录项

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号