Mizuno Yukio, Mori-Yoshimura Madoka, Oya Yasushi, Nishikawa Atsuko, Nishino Ichizo, Takahashi Yuji
Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry.
Department of Neurology, Yokohama Asahi Chuo General Hospital.
Rinsho Shinkeigaku. 2017 Nov 25;57(11):691-697. doi: 10.5692/clinicalneurol.cn-001024. Epub 2017 Oct 26.
Nemaline myopathy commonly presents with symmetrical proximal weakness. Here we report two cases of nemaline myopathy presenting with distal dominant involvement with prominent asymmetry. Case 1 was a 37-year-old man who recalled frequently falling down and had right calf atrophy since he was 3-years-old. He had right calf muscle atrophy and weakness and steppage gait; his cardiopulmonary function was normal. Case 2 was a 35-year-old man with right calf muscle atrophy and weakness since childhood. He had right dominant distal leg weakness and atrophy together with respiratory failure and started noninvasive positive pressure ventilation. He also developed cardiomyopathy and died from acute respiratory failure due to pneumonia at age 39. Both cases harbored compound heterozygous nebulin (NEB) mutations with c.20131 C>T:p.Arg6711Trp and a nonsense mutation. Nemaline myopathy associated with NEB mutations can present as distal dominant myopathy with prominent asymmetry.
杆状体肌病通常表现为对称性近端肌无力。在此,我们报告两例杆状体肌病,其以远端为主受累且伴有明显不对称性。病例1为一名37岁男性,自3岁起就经常摔倒,右小腿萎缩。他右小腿肌肉萎缩且无力,呈跨阈步态;心肺功能正常。病例2为一名35岁男性,自幼右小腿肌肉萎缩且无力。他以右侧为主的小腿远端肌无力和萎缩,伴有呼吸衰竭,并开始接受无创正压通气治疗。他还发展为心肌病,39岁时因肺炎导致急性呼吸衰竭死亡。两例均携带复合杂合性伴肌动蛋白(NEB)突变,即c.20131 C>T:p.Arg6711Trp和一个无义突变。与NEB突变相关的杆状体肌病可表现为以远端为主的肌病,并伴有明显不对称性。