Piggott H
J Bone Joint Surg Br. 1980 Feb;62-B(1):54-8. doi: 10.1302/0301-620X.62B1.6985915.
Two hundred and fifty cases of myelodysplasia were reviewed in relation to spinal deformity. Approximately half of the children had, or were expected to develop, curves severe enough to need operations and only 10 per cent maintained completely undeformed spines. The most frequent deformity was scoliosis which could be subdivided into congenital and developmental types. The latter was of mixed aetiology, neuromuscular imbalance and asymmetry of the neural arch both contributing, while in some cases no causative factors could be identified. The best early indicator that developmental scoliosis was likely to appear was a high segmental level of both the neurological deficit and the neural arch defect. Deformity was very unlikely to start after the age of nine years.
对250例骨髓发育异常患者的脊柱畸形情况进行了回顾性研究。大约一半的儿童已经出现或预计会发展出严重到需要手术治疗的脊柱侧弯,只有10%的儿童脊柱能完全保持无畸形状态。最常见的畸形是脊柱侧弯,可分为先天性和发育性两种类型。发育性脊柱侧弯病因复杂,神经肌肉失衡和神经弓不对称都有影响,在某些情况下无法确定病因。发育性脊柱侧弯可能出现的最佳早期指标是神经功能缺损和神经弓缺陷的节段位置较高。9岁以后很少会出现脊柱畸形。