1 Neurologisk Klinik, Neurocentret, Rigshospitalet, The Capital Region of Denmark2 Klinisk Neurofysiologisk Klinik, Neurocentret, Rigshospitalet, The Capital Region of Denmark
Lambert-Eaton myasthenic syndrome (LEMS) is a rare condition, which may mimic myopathy. A few reports have described that EMG in LEMS may show changes compatible with myopathy, and muscle biopsies have been described with type II as well as type I atrophy. The EMG results were, however, based on qualitative EMG examination and the histopathological methods were not always clear. The objective of this study was to investigate if the previous EMG findings could be confirmed with quantitative EMG (QEMG) and to describe muscle histology in LEMS.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology, 2013, Vol 124, Issue 9, p. 1889-92