Scott R M, Wolpert S M, Bartoshesky L E, Zimbler S, Karlin L
Department of Neurosurgery, New England Medical Center, Boston, Massachusetts.
Neurosurgery. 1988 Apr;22(4):739-44. doi: 10.1227/00006123-198804000-00021.
Segmental spinal dysgenesis is characterized by focal agenesis or dysgenesis of the lumbar or thoracolumbar spine, with focal abnormality of the underlying spinal cord and nerve roots. Children are symptomatic at birth with lower limb deformities and neurological deficits that may be segmental. Myelography and computed tomography disclose hypoplastic or absent vertebrae and atrophic or absent neural elements adjacent to the bony deformity; the spinal column distal to the abnormality may be partially bifid, but is otherwise normal. Spinal ultrasonography was a helpful diagnostic adjunct in one patient. Surgery may be helpful in decompressing partially functioning spinal cord or nerve roots, but may exaggerate the tendency toward spinal instability. The embryology of this abnormality is not clear, but two children had other anomalies suggesting a spinal dysraphic syndrome, and its cause is probably related to a segmental maldevelopment of the neural tube.
节段性脊柱发育不全的特征是腰椎或胸腰段脊柱局部发育不全或发育异常,同时伴有脊髓和神经根的局部异常。患儿出生时即出现症状,表现为下肢畸形和可能呈节段性分布的神经功能缺损。脊髓造影和计算机断层扫描显示椎体发育不全或缺失,以及与骨畸形相邻的神经组织萎缩或缺失;畸形远端的脊柱可能部分呈双裂,但其他方面正常。脊柱超声检查对1例患者的诊断有辅助作用。手术可能有助于解除部分功能的脊髓或神经根的压迫,但可能会加重脊柱不稳定的倾向。这种异常的胚胎学机制尚不清楚,但有2例患儿伴有其他畸形,提示为脊柱闭合不全综合征,其病因可能与神经管的节段性发育异常有关。