Yu Xue-Fan, Miao Jing, Li Yan, Jiang Xin-Mei, Ma Yu-Gang, Meng Hong-Mei
Department of Neurology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Exp Ther Med. 2015 Feb;9(2):432-434. doi: 10.3892/etm.2014.2140. Epub 2014 Dec 16.
Myoclonic epilepsy with ragged-red fibers is a maternally inherited disease that is characterized by myoclonic epilepsy, cerebellar ataxia and progressive muscular weakness. The present study reports the case of a 25-year-old male who presented with paroxysmal left upper limb tics and weakness for two years. Neurological examination revealed intact cranial nerves, decreased deep tendon reflexes and decreased sensation of touch, pain and vibration. The gait of the patient was broad and he was unable to walk in a straight line. Local cortical atrophy was also observed in the left temporal-occipital cortex on a magnetic resonance imaging scan. The muscle biopsy revealed ragged-red fibers. Therefore, the present study hypothesized that imaging observations and follow-up examinations are important in patients with myoclonic epilepsy.
肌阵挛性癫痫伴破碎红纤维病是一种母系遗传疾病,其特征为肌阵挛性癫痫、小脑共济失调和进行性肌肉无力。本研究报告了一名25岁男性的病例,该患者出现阵发性左上肢抽搐和无力症状达两年。神经系统检查显示颅神经正常、深部腱反射减弱以及触觉、痛觉和振动觉减退。患者步态宽基,无法直线行走。磁共振成像扫描还观察到左侧颞枕叶皮质局部萎缩。肌肉活检显示有破碎红纤维。因此,本研究推测影像学观察和随访检查对肌阵挛性癫痫患者很重要。