Wright K C, Ramsey-Goldman R, Nielsen V K, Nicholas J J
University of Pittsburgh Medical School, PA 15213.
Arch Phys Med Rehabil. 1988 Jul;69(7):534-6.
In 1979 Wiechers and Johnson described ten patients with diffuse abnormal insertional activity on EMG examination in the absence of neuromuscular disease. We present a family group with identical findings. The propositus is a 53-year-old woman who presented with back pain. EMG studies revealed trains of positive sharp waves with needle movement in all muscles studied. Nerve conduction studies, radiographs, and laboratory studies were all unremarkable. We recruited eight additional family members who underwent a screening EMG of five muscles. Four patients had trains of positive sharp waves present in all five muscles. To our knowledge, this is the first report confirming the findings of Wiechers and Johnson. We concur with them that the abnormality appears to be genetically transmitted in an autosomal dominant pattern. Although without clinical significance, it is important for electromyographers to be aware of this entity so as not to mistakenly ascribe serious neuromuscular disease to these patients.
1979年,维彻斯和约翰逊描述了10例在肌电图检查中存在弥漫性异常插入活动但无神经肌肉疾病的患者。我们展示了一个有相同发现的家族群体。先证者是一名53岁的女性,她因背痛前来就诊。肌电图研究显示,在所研究的所有肌肉中,针移动时均出现一连串正锐波。神经传导研究、X光片和实验室检查均无异常。我们招募了另外8名家庭成员,对其5块肌肉进行了筛查性肌电图检查。4名患者的所有5块肌肉中均出现了一连串正锐波。据我们所知,这是第一份证实维彻斯和约翰逊研究结果的报告。我们同意他们的观点,即这种异常似乎以常染色体显性模式进行遗传传递。尽管没有临床意义,但肌电图检查人员了解这一情况很重要,以免将严重的神经肌肉疾病错误地归因于这些患者。