Division of Clinical Neurophysiology, Department of Neurology,University of Health Sciences Adana City Training and Research Hospital, Adana, Turkey.
Department of Neurology, University of Health Sciences Adana City Training and Research Hospital, Adana, Turkey.
Turk J Med Sci. 2023 Feb;53(1):233-242. doi: 10.55730/1300-0144.5578. Epub 2023 Feb 22.
: Needle electromyography (EMG) abnormalities in the trapezius muscle (TM) can be seen in neuromuscular disorders. The aim was to determine the characteristics of needle EMG abnormalities observed in the TM in neuromuscular disorders.
The data of patients who applied to the Clinical Neurophysiology Laboratory of University of Health Sciences Adana City Training and Research Hospital between December 2018 and October 2021 were reviewed. Polio survivors, amyotrophic lateral sclerosis (ALS) patients, patients with sensorimotor polyneuropathy, patients with spinal cord lesions involving C2/C3/C4 segments, patients with spinal accessory nerve (SAN) lesions, neuralgic amyotrophy (NA) patients, and patients with myopathy were included. Needle EMG findings of the upper TM of the patients were analyzed. Positive sharp waves, fibrillation potentials, fasciculation potentials, myotonic discharges, and motor unit action potential (MUAP) changes were considered needle EMG abnormalities.
Eighty-one polio survivors, 23 ALS patients, 39 patients with sensorimotor polyneuropathy, 10 patients with cervical spinal lesions, eight NA patients, seven patients with SAN lesions, and three patients with myopathy were included in the study. Fifteen (65.2%) ALS patients, 18 (22.2%) polio survivors, three (30%) patients with cervical spinal lesions, two (5.1%) patients with sensorimotor neuropathy, one (12.5%) NA patient, seven (100%) patients with SAN lesions, and two (66.7%) patients with myopathies had at least one needle EMG abnormality in the TM. Fasciculation potentials in the TM were seen in 10 (43.5%) ALS patients. In four patients with SAN lesions and one polio survivor, MUAP could not be obtained from the TM.
There may be more frequent needle EMG abnormalities, particularly in ALS patients and patients with SAN lesions. Since the number of patients with myopathy included in this study was low, it is difficult to comment on the needle EMG features of the TM for these patients. In addition, this study indicated that fasciculation potentials in the TM are typical in ALS patients and that MUAP may not be obtained from the TM in patients with SAN lesions.
斜方肌(TM)的针极肌电图(EMG)异常可见于神经肌肉疾病。本研究旨在确定神经肌肉疾病中 TM 针极 EMG 异常的特征。
回顾 2018 年 12 月至 2021 年 10 月期间在阿德亚曼城市健康科学大学附属医院临床神经生理学实验室就诊的患者数据。纳入的患者包括脊髓灰质炎幸存者、肌萎缩侧索硬化症(ALS)患者、感觉运动性多神经病患者、累及 C2/C3/C4 节段的脊髓病变患者、副神经(SAN)病变患者、神经痛性肌萎缩(NA)患者和肌病患者。分析患者上斜方肌的针极 EMG 发现。阳性尖波、纤颤电位、束颤电位、肌强直放电和运动单位动作电位(MUAP)改变被认为是针极 EMG 异常。
本研究纳入了 81 例脊髓灰质炎幸存者、23 例 ALS 患者、39 例感觉运动性多神经病患者、10 例颈椎病变患者、8 例 NA 患者、7 例 SAN 病变患者和 3 例肌病患者。15 例(65.2%)ALS 患者、18 例(22.2%)脊髓灰质炎幸存者、3 例(30%)颈椎病变患者、2 例(5.1%)感觉运动性神经病患者、1 例(12.5%)NA 患者、7 例(100%)SAN 病变患者和 2 例(66.7%)肌病患者的 TM 至少有一项针极 EMG 异常。10 例(43.5%)ALS 患者的 TM 中可见束颤电位。4 例 SAN 病变患者和 1 例脊髓灰质炎幸存者的 TM 无法获得 MUAP。
TM 的针极 EMG 异常可能更为常见,尤其是在 ALS 患者和 SAN 病变患者中。由于纳入本研究的肌病患者数量较少,因此难以对这些患者的 TM 针极 EMG 特征进行评论。此外,本研究表明,TM 中的束颤电位是 ALS 患者的典型表现,SAN 病变患者的 TM 可能无法获得 MUAP。