Gérard J M, Telerman-Toppet N, Borenstein S, Flament-Durand J
Service de Neurologie et d'Anatomo-Pathologie, Hôpital Erasme, Bruxelles.
Rev Neurol (Paris). 1991;147(2):144-7.
An unusual myopathy with extensive myofibrillar degeneration related to the Z disk is reported. Focal Z disk disappearance, accumulation of numerous rods and cytoplasmic bodies and some rimmed vacuoles represented the major pathologic features of this sporadic muscular disorder, sharing common clinical and electrophysiological features with inclusion body myositis. This diagnosis was excluded because all nuclei appeared normal and 15-18 nm filaments were not observed in cytoplasm or in the vicinity of membranous whorls. Intramuscular innervation was studied by vital staining with methylene blue: the terminal innervation ratio was normal, indicating a myopathic disorder. The relationship between the present disorder and cytoplasmic bodies and nemaline myopathies is discussed.
报道了一种与Z盘相关的具有广泛肌原纤维变性的罕见肌病。局灶性Z盘消失、大量杆状体和胞质体聚集以及一些镶边空泡是这种散发性肌肉疾病的主要病理特征,与包涵体肌炎具有共同的临床和电生理特征。由于所有细胞核均正常,且在细胞质或膜性涡旋附近未观察到15 - 18纳米的细丝,故排除了该诊断。通过亚甲蓝活体染色研究肌肉内神经支配:终末神经支配率正常,提示为肌病性疾病。讨论了目前这种疾病与胞质体和杆状体肌病之间的关系。