Ikeuchi T, Anezaki T, Ishiguro H, Tanaka M, Tanaka K, Tsuji S
Department of Neurology, Brain Research Institute, Niigata University.
Rinsho Shinkeigaku. 1995 Sep;35(9):1016-20.
We reported two siblings with slowly progressive muscle weakness in proximal and peroneal muscles without atrophy, myalgia, cramps, or episodic weakness. The serum creatine kinase level was moderately elevated. The prominent features of their muscle pathology were accumulation of tubular aggregates in type 2 fibers, predominantly in type 2B fibers, and marked type 1 fiber atrophy. Three to eleven % of muscle fibers contained tubular aggregates. Electron microscopic examination revealed accumulation of double-walled tubular structures. Familial myopathy with tubular aggregates as a hallmark of muscle pathology is considered to be a new clinical form of childhood-onset familial myopathies.
我们报告了两名患有近端和腓骨肌缓慢进行性肌无力的兄弟姐妹,无萎缩、肌痛、痉挛或发作性肌无力。血清肌酸激酶水平中度升高。其肌肉病理的突出特征是2型纤维中管状聚集体的积累,主要在2B型纤维中,以及明显的1型纤维萎缩。3%至11%的肌纤维含有管状聚集体。电子显微镜检查显示双壁管状结构的积累。以管状聚集体为肌肉病理特征的家族性肌病被认为是儿童期起病的家族性肌病的一种新的临床形式。