Werneck L C, Lima J G
Internal Medicine Department, Universidade Federal do Paraná, Curitiba, PR Brasil.
Arq Neuropsiquiatr. 1988 Jun;46(2):156-65. doi: 10.1590/s0004-282x1988000200006.
To find what the correlation is and verify if it is possible to avoid extensive electromyographic examination, studying only one muscle, 100 patients with neuromuscular disorders (58 primary myopathies, 32 neurogenic disorders and 10 myotonic dystrophies) were submitted to quantified electromyography (EMG) and muscle biopsy (MB) with fresh-frozen section plus histochemistry in the same muscle, but on the opposite side. The EMG was abnormal in 98% and MB in 93% of the cases. EMG and MB had a concordance of 84.3% in the neurogenic disorders and 84.77% in the primary myopathies. A correlation of 80% was obtained between all MB and EMG (including the cases of myotonic dystrophies), regarding the origin of the pathogenic process (p less than 0.01). The EMG had 5% inconsistencies and the MB 11%, with respect to the pathogenic process. When the myotonic dystrophy was separated from the primary myopathies and from the denervation disorders, a complete concordance was found in all MB and had only 3.4% inconsistencies in the denervation disorders and 3.1% in the primary myopathies.
为了确定相关性,并验证仅通过研究一块肌肉来避免进行广泛的肌电图检查是否可行,对100例神经肌肉疾病患者(58例原发性肌病、32例神经源性疾病和10例强直性肌营养不良症)进行了定量肌电图(EMG)检查,并在同一肌肉的对侧进行了新鲜冷冻切片加组织化学的肌肉活检(MB)。98%的病例EMG异常,93%的病例MB异常。在神经源性疾病中,EMG和MB的一致性为84.3%,在原发性肌病中为84.77%。就致病过程的起源而言,所有MB和EMG之间(包括强直性肌营养不良症病例)的相关性为80%(p小于0.01)。就致病过程而言,EMG有5%的不一致性,MB有11%的不一致性。当将强直性肌营养不良症与原发性肌病和去神经疾病分开时,所有MB完全一致,在去神经疾病中仅有3.4%的不一致性,在原发性肌病中有3.1%的不一致性。