Tanaka A
Nihon Seikeigeka Gakkai Zasshi. 1986 Dec;60(12):1227-38.
To elucidate morphologic events, 105 intervertebral discs in 22 patients with idiopathic scoliosis and 14 in four patients with paralytic scoliosis were histopathologically compared with 13 control intervertebral discs in 13 cases, including three fetuses. In control intervertebral discs, the notochordal area became smaller with age, and was almost completely occupied by fibrocartilagenous matrix at 16 years of age or more. In intervertebral discs of patients aged 19-33 with idiopathic scoliosis, many notochordal cells were seen and many areas without fibrocartilagenous matrix were found. In contrast, in intervertebral discs of patients aged 21-35 with paralytic scoliosis, there was no notochordal cells or defect of the fibrocartilagenous matrix. The results suggest an impairment of transition from the notochordal nucleus to the fibrocartilagenous nucleus in intervertebral discs in patients with idiopathic scoliosis, and that such abnormalities are related to the onset of idiopathic scoliosis.
为阐明形态学变化,对22例特发性脊柱侧凸患者的105个椎间盘和4例麻痹性脊柱侧凸患者的14个椎间盘进行了组织病理学检查,并与13例对照者(包括3例胎儿)的13个椎间盘进行了比较。在对照椎间盘中,脊索区随年龄增长而变小,在16岁及以上时几乎完全被纤维软骨基质占据。在19 - 33岁特发性脊柱侧凸患者的椎间盘中,可见许多脊索细胞,且发现许多无纤维软骨基质的区域。相比之下,在21 - 35岁麻痹性脊柱侧凸患者的椎间盘中,没有脊索细胞,也没有纤维软骨基质缺陷。结果表明,特发性脊柱侧凸患者椎间盘中从脊索核向纤维软骨核的转变存在损害,且这种异常与特发性脊柱侧凸的发病有关。