Krarup C, Stewart J D, Sumner A J, Pestronk A, Lipton S A
Department of Medicine, Brigham and Women's Hospital, Boston, MA.
Neurology. 1990 Jan;40(1):118-27. doi: 10.1212/wnl.40.1.118.
We describe 3 patients with asymmetric limb weakness, fasciculations (2 patients), relatively preserved reflexes, normal cranial nerves, and few or no sensory abnormalities. The symptoms had been progressive over 1 to 15 years. Detailed motor nerve conduction studies showed conduction block and slowing localized to sharply circumscribed areas 30 to 100 mm long in several nerves in each patient. By contrast, the sensory conduction studies over the same nerve segments were normal, indicating very selective involvement of motor fibers. Sural nerve biopsies showed minor changes that varied among the patients. One patient had high levels of anti-GM1 antibodies, 1 had mildly elevated levels, and 1 had high levels of only asialo-GM1 antibodies. Treatment with immune suppressive therapy has produced minimal improvement in 1 patient.
我们描述了3例患者,他们有不对称肢体无力、肌束震颤(2例)、相对保留的反射、正常的颅神经以及很少或没有感觉异常。症状在1至15年中呈进行性发展。详细的运动神经传导研究显示,传导阻滞和减慢局限于每位患者数条神经中30至100毫米长的界限分明的区域。相比之下,同一神经节段的感觉传导研究正常,表明运动纤维有非常选择性的受累。腓肠神经活检显示患者之间存在轻微差异。1例患者抗GM1抗体水平高,1例轻度升高,1例仅唾液酸缺乏GM1抗体水平高。免疫抑制治疗仅使1例患者有轻微改善。