Ozerdemoglu Remzi A, Denis Francis, Transfeldt Ensor E
Department of Orthopaedics and Traumatology, Süleyman Demirel University, Isparta, Turkey.
Spine (Phila Pa 1976). 2003 Jul 1;28(13):1410-7. doi: 10.1097/01.BRS.0000067117.07325.86.
A retrospective review with statistical correlations of 112 patients having both scoliosis and syringomyelia was performed.
To determine whether there were significant correlations between the type of scoliosis, location of the syrinx, size of the syrinx, clinical manifestation of the syrinx, and associated lesions such as cord tethering and Chiari malformation (Chiari I or Arnold-Chiari II).
The coexistence of scoliosis and syringomyelia has been described previously, but these detailed correlations have had minimal attention.
All patients at the center with scoliosis of any type plus a syrinx had a detailed chart and radiologic review coupled with detailed statistical analysis.
Scoliosis and syringomyelia were seen in four diagnoses: myelomeningocele, myelomeningocele with congenital scoliosis, congenital scoliosis, and scoliosis with neither congenital anomalies nor myelomeningocele. Chiari malformation and cord tethering appear to have a major relation to scoliosis with syringomyelia.
Anomalies of the spinal cord or spinal column coexisting with lesions of the central nervous system have significant effects on the syrinx and scoliosis. There is a significant relation between the most caudal level of the syrinx and the locations of the scoliosis.
对112例同时患有脊柱侧弯和脊髓空洞症的患者进行了回顾性研究并进行统计学相关性分析。
确定脊柱侧弯类型、脊髓空洞位置、脊髓空洞大小、脊髓空洞临床表现以及诸如脊髓栓系和Chiari畸形(Chiari I型或Arnold-Chiari II型)等相关病变之间是否存在显著相关性。
脊柱侧弯和脊髓空洞症的共存此前已有描述,但这些详细的相关性很少受到关注。
该中心所有患有任何类型脊柱侧弯加脊髓空洞症的患者均进行了详细的病历和影像学检查,并进行了详细的统计分析。
在四种诊断中发现了脊柱侧弯和脊髓空洞症:脊髓脊膜膨出、伴有先天性脊柱侧弯的脊髓脊膜膨出、先天性脊柱侧弯以及既无先天性异常也无脊髓脊膜膨出的脊柱侧弯。Chiari畸形和脊髓栓系似乎与伴有脊髓空洞症的脊柱侧弯有主要关系。
脊髓或脊柱的异常与中枢神经系统病变共存对脊髓空洞症和脊柱侧弯有显著影响。脊髓空洞最尾端水平与脊柱侧弯位置之间存在显著关系。