Yoneyama H, Kohno Y, Nonaka I
Department of Pediatrics, Kitakyushu City Ryoiku Center, Fukuoka.
No To Hattatsu. 1993 Jul;25(4):374-8.
A 10-year-old boy with rigid spine syndrome was reported. He had mild weakness in the limb, and moderate weakness in the neck flexor and extensor muscles since early childhood. Because of limited flexion of the spine, he could not bend down. CT of the muscles revealed increased low density in the erector spine muscle, predominantly at the lumbar level. In the biopsy specimens obtained from the left biceps brachii and erector spine muscles, there was a variation in fiber size with scattered necrotic and regenerating fibers, and fibrosis, predominantly in the latter. Except for scattered fibers with rimmed vacuoles, the overall histopathological features were similar to those seen in progressive muscular dystrophies, suggesting that the dystrophic process is one of the major pathomechanisms for rigid spine syndrome.
报道了一名患有僵硬脊柱综合征的10岁男孩。自幼年起,他肢体有轻度无力,颈部屈肌和伸肌有中度无力。由于脊柱屈曲受限,他无法弯腰。肌肉CT显示竖脊肌低密度增加,主要在腰椎水平。在从左肱二头肌和竖脊肌获取的活检标本中,纤维大小存在差异,有散在的坏死和再生纤维,以及纤维化,以后者为主。除了有边缘空泡的散在纤维外,总体组织病理学特征与进行性肌营养不良所见相似,提示营养不良过程是僵硬脊柱综合征的主要发病机制之一。