Keller Christian E, Hays Arthur P, Rowland Lewis P, Moghadaszadeh Behzad, Beggs Alan H, Bhagat Govind
Department of Pathology, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
Arch Neurol. 2006 Jan;63(1):132-4. doi: 10.1001/archneur.63.1.132.
A 45-year-old man with severe proximal muscle weakness had findings diagnostic of adult-onset nemaline myopathy. He also had a monoclonal gammopathy. This is the fifth report of adult-onset nemaline myopathy in a patient with monoclonal gammopathy, suggesting that the occurrence of these entities may be more than a chance association. Myocyte-bound immunoglobulin or light chains were not detected and immunotherapy was not effective in this patient. Other causes of adult-onset nemaline myopathy were ruled out, including the most common mutations of sarcomeric thin filament genes.
一名45岁男性,近端肌肉严重无力,检查结果诊断为成人起病的杆状体肌病。他还患有单克隆丙种球蛋白病。这是关于成人起病的杆状体肌病合并单克隆丙种球蛋白病患者的第五份报告,提示这些病症的出现可能并非偶然关联。该患者未检测到肌细胞结合免疫球蛋白或轻链,免疫治疗也无效。已排除成人起病的杆状体肌病的其他病因,包括肌节细肌丝基因最常见的突变。