Matsumoto Chihiro, Mori-Yoshimura Madoka, Noguchi Satoru, Endo Yukari, Oya Yasushi, Murata Miho, Nishino Ichizo, Takahashi Yuji
Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry, 4-1-1 Ogawahigashi, Kodaira, Tokyo 187-8551, Japan.
Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry, 4-1-1 Ogawahigashi, Kodaira, Tokyo 187-8551, Japan.
Brain Dev. 2019 May;41(5):470-473. doi: 10.1016/j.braindev.2018.12.002. Epub 2019 Mar 4.
We report a 38-year-old woman who presented with mild proximal dominant muscle weakness and fatigability that fluctuated during menstruation and treatment with ephedrine-containing medication. The patient had been diagnosed with "congenital myopathy with tubular aggregates" by muscle biopsy at age 19. Her revised diagnosis was congenital myasthenic syndrome (CMS) caused by a mutation in GFPT1 (2p13.3 [MIM 610542], c.722_723insG homozygote, CMS-GFPT1) based on a screening gene analysis. Muscle CT revealed diffuse atrophy of proximal and axial muscles focused on the vastus lateralis, hamstrings, medial gastrocnemius and soleus muscles. Oral administration of pyridostigmine bromide clearly ameliorated weakness and fatigability. This is the first reported case of CMS-GFPT1 in Japan. Since CMS symptoms are reactive to treatment, it is important for clinicians to make an accurate diagnosis at an early stage to improve patient QOL. Tubular aggregates in muscle biopsy and day-to-day fluctuations are important features of the disorder. Quantitative muscle strength measurement was effective for evaluating treatment efficacy.
我们报告了一名38岁女性,她表现为轻度近端为主的肌肉无力和疲劳,在月经期间以及使用含麻黄碱药物治疗时症状会波动。该患者19岁时经肌肉活检被诊断为“伴有管状聚集物的先天性肌病”。基于筛查基因分析,她的修订诊断为GFPT1基因(2p13.3 [MIM 610542],c.722_723insG纯合子,CMS - GFPT1)突变导致的先天性肌无力综合征(CMS)。肌肉CT显示近端和轴性肌肉弥漫性萎缩,主要集中在股外侧肌、腘绳肌、腓肠肌内侧头和比目鱼肌。口服溴吡斯的明明显改善了无力和疲劳症状。这是日本首例报道的CMS - GFPT1病例。由于CMS症状对治疗有反应,临床医生早期准确诊断对于改善患者生活质量很重要。肌肉活检中的管状聚集物和日常波动是该疾病的重要特征。定量肌肉力量测量对于评估治疗效果有效。