Puri V, Chaudhry N, Jain K K, Chowdhury D, Nehru R
Department of Neurology, G.B. Pant Hospital, New Delhi 110002, India.
Electromyogr Clin Neurophysiol. 2004 Jun;44(4):229-35.
A retrospective study to evaluate the clinical and electrophysiological profile of brachial plexus lesions in a tertiary care center of India.
Thirty eight patients with brachial plexopathy (idiopathic or traumatic) with detailed electrophysiological studies were sampled. This included detailed motor and sensory nerve conduction studies of the conventional median, ulnar and radial nerves of the upper limbs, CMAP from deltoid, biceps and triceps on stimulating the ERB's point, needle EMG in the appropriate muscles and paraspinal muscles. The electrophysiological studies were performed on both sides irrespective of the clinical involvement and were recorded within 1.61 +/- 2.89 months in idiopathic group and 2.11 +/- 2.65 months in traumatic plexopathy group. The severity of involvement was assessed on MRC scale. ADL scale was used to assess the disability at presentation and subsequent follow up.
12 patients (11 male and 01 female) had idiopathic brachial plexopathy and 26 patients (all male) had traumatic brachial plexopathy. In the idiopathic group the lesion was localized to upper trunk in 58.3% of patients and middle trunk (posterior cord) in 41.66% and none had lower trunk or diffuse involvement. 25% had bilateral involvement. Two patients (16.6%) with idiopathic plexitis had recurrence involving the opposite side during the follow up. In the traumatic group the lesion was localized to the upper trunk in 11.53%, middle trunk (posterior cord) in 57.69% and 30.76% of patients had diffuse involvement. All the patients in traumatic plexopathy group had severe disability while in idiopathic group 91.66% had severe disability and 8.33% had moderate disability. Low amplitude CMAP and F wave abnormality were seen in 16.6% of patients in idiopathic group. On needle EMG 83.3% had fasciculation or fibrillations while none had paraspinal EMG abnormality. In traumatic group low to absent CMAP was seen in 69.2% and 76.92% had F wave abnormality. SNAPs were not recordable in 53.8%. On Needle EMG all the patients showed fasciculation or fibrillations and only 6 (23.0%) had paraspinal muscle fibrillations. Root avulsion could be documented in only four of these cases on MR imaging.
Recovery in the traumatic group correlated well with the electrophysiological abnormalities while no such correlation was evident in the idiopathic group.
一项回顾性研究,旨在评估印度一家三级医疗中心臂丛神经损伤的临床和电生理特征。
选取38例患有臂丛神经病变(特发性或创伤性)且进行了详细电生理研究的患者。这包括对上肢常规正中神经、尺神经和桡神经进行详细的运动和感觉神经传导研究,刺激埃尔布点时三角肌、肱二头肌和肱三头肌的复合肌肉动作电位(CMAP),在适当肌肉和椎旁肌进行针极肌电图检查。无论临床受累情况如何,均对双侧进行电生理研究,特发性组在1.61±2.89个月内记录,创伤性臂丛神经病变组在2.11±2.65个月内记录。根据医学研究委员会(MRC)量表评估受累严重程度。使用日常生活活动(ADL)量表评估就诊时及随后随访时的残疾情况。
12例患者(11例男性和1例女性)患有特发性臂丛神经病变,26例患者(均为男性)患有创伤性臂丛神经病变。在特发性组中,58.3%的患者病变局限于上干,41.66%局限于中干(后束),无一例患者有下干或弥漫性受累。25%有双侧受累。2例(16.6%)特发性臂丛神经炎患者在随访期间对侧复发。在创伤性组中,11.53%的患者病变局限于上干,57.69%局限于中干(后束),30.76%的患者有弥漫性受累。创伤性臂丛神经病变组所有患者均有严重残疾,而特发性组91.66%有严重残疾,8.33%有中度残疾。特发性组16.6%的患者出现复合肌肉动作电位波幅降低和F波异常。针极肌电图检查显示83.3%有肌束震颤或纤颤,无一例椎旁肌电图异常。在创伤性组中,69.2%出现复合肌肉动作电位波幅降低或消失,76.92%有F波异常。53.8%无法记录感觉神经动作电位(SNAPs)。针极肌电图检查所有患者均有肌束震颤或纤颤,仅6例(23.0%)有椎旁肌纤颤。在这些病例中,仅4例通过磁共振成像记录到神经根撕脱。
创伤性组的恢复与电生理异常密切相关,而在特发性组中未发现这种相关性。