Yarom R, Robin G C
Isr J Med Sci. 1979 Nov;15(11):917-24.
Muscles from patients with scoliosis were studied to determine the possible relationship between neuromuscular disease and idiopathic scoliosis. Biopsies taken from the paraspinal musculature, the gluteus maximus and other sites were examined and compared with control specimens taken from patients undergoing spinal surgery for other disorders. Morphological and morphometric examinations by light and electron microscopy revealed a wide range of pathological changes and an alteration in the normal distribution of fiber types in most muscles. Changes were mainly nonspecific, but one unusual feature in idiopathic scoliosis but not in the other types of scoliosis consisted of type I fiber atrophy in paraspinal and deltoid muscles of the concave side paraspinal muscle, the site of the maximum morphological changes. The localized muscle changes, which are disease and not deformity related, suggest that idiopathic scoliosis is a separate disease entity and that the central nervous system may be involved in its genesis.
对脊柱侧弯患者的肌肉进行了研究,以确定神经肌肉疾病与特发性脊柱侧弯之间可能存在的关系。取自椎旁肌肉组织、臀大肌和其他部位的活检样本进行了检查,并与因其他疾病接受脊柱手术的患者的对照样本进行了比较。通过光镜和电镜进行的形态学和形态计量学检查显示,大多数肌肉存在广泛的病理变化以及纤维类型正常分布的改变。这些变化主要是非特异性的,但特发性脊柱侧弯中一个不寻常的特征(而其他类型的脊柱侧弯中没有)是凹侧椎旁肌、椎旁肌和三角肌中I型纤维萎缩,该部位有最大的形态学变化。这些局部肌肉变化与疾病而非畸形相关,表明特发性脊柱侧弯是一种独立的疾病实体,并且中枢神经系统可能参与其发病过程。