Coërs C, Telerman-Toppet N, Gérard J M, Szliwowski H, Bethlem J, van Wijngaarden G K
Neurology. 1976 Nov;26(11):1046-53. doi: 10.1212/wnl.26.11.1046.
Changes in motor innervation were compared with histologic and histochemical pattern of muscle fibers in three biopsies of central core disease, four biopsies of nemaline myopathy, one biopsy of myotubular myopathy, and three biopsies of mitochondrial myopathy. Evidence of collateral reinnervation was obtained only in one biopsy from central core disease. In other biopsies, no structural or ultrastructural abnormality of axis cylinders, myelin, or myoneural junction suggesting denervation were observed. The only relevant change found in centronuclear myopathy and to a lesser extent in nemaline myopathy was an unusual smallness and simplication of motor endings, suggesting delayed or impaired maturation. Muscle fibers strongly reactive for both adenosinetriphosphatase and nicotinamide-adenine dinucleotide diaphorase, observed in central core disease and mitochondrial myopathy, were not associated with increased terminal innervation ratio.
对3例中央轴空病、4例杆状体肌病、1例肌管性肌病和3例线粒体肌病的活检样本,比较了运动神经支配的变化与肌纤维的组织学和组织化学模式。仅在1例中央轴空病的活检样本中发现了侧支神经再支配的证据。在其他活检样本中,未观察到轴突、髓鞘或肌神经连接的结构或超微结构异常提示失神经支配。在中央核性肌病中发现的唯一相关变化,以及在杆状体肌病中程度较轻的变化,是运动终末异常细小和简单化,提示成熟延迟或受损。在中央轴空病和线粒体肌病中观察到的对三磷酸腺苷酶和烟酰胺腺嘌呤二核苷酸黄递酶均有强烈反应的肌纤维,与终末神经支配率增加无关。