Sarwark J F, Weber D T, Gabrieli A P, McLone D G, Dias L
Northwestern University Medical School, Children's Memorial Hospital, Chicago, Ill., USA.
Pediatr Neurosurg. 1996 Dec;25(6):295-301. doi: 10.1159/000121143.
The clinical presentation of tethered spinal cord and the results of tethered cord release were examined in a group of 30 low motor level (L3 and below) children with a history of myelomeningocele without concomitant CNS complications. Changes in orthopedic and/or neurologic status formed the basis of consideration for tethered cord release. Clinically, these patients presented with a new onset or recently progressing scoliosis, spasticity with or without contractures, decrease in motor function and low back pain at the site of closure. One or more of these findings was present in all cases and led to the suspicion of tethered spinal cord. The diagnosis of tethered cord was confirmed in all cases by MRI or CT myeolography. In order to isolate tethering as the etiology for the patients' clinical deterioration, patients with concomitant CNS complications, e.g. shunt dysfunction or hydromyelia were excluded from the study. Twenty-nine such patients, of an initial 59, who would have otherwise been considered, were excluded on the basis of this criteria of concomitant CNS complications. The results of release 1 year after the procedure were as follows: regarding scoliosis, in 75% of cases the curve either remained stable or decreased by more than 10 degrees, with 25% experiencing curve progression of > 10 degrees. The most recent follow-up in this group revealed that 11.8% experienced a decrease in curvature of >10 degrees; 47.1% remained stable, and 41.2% ultimately progressed 10 degrees. In the group with spasticity, 43.8% improved; 56.3% remained stable, and none worsened. Most (78.6%) of the children who had experienced a decline in motor function improved postoperatively, and all those with back pain experienced complete resolution. In conclusion, tethered cord release in symptomatic low lumbar and sacral level children with myelomeningocele appears to be of benefit, especially with respect to stabilization of scoliosis in selected patients, back pain at the site of closure, and prior decline in motor function. Results in the cases with spasticity were more equivocal.
对一组30名运动水平较低(L3及以下)、有脊髓脊膜膨出病史且无中枢神经系统并发症的儿童,检查其脊髓拴系的临床表现及脊髓拴系松解术的结果。矫形和/或神经状态的变化是考虑进行脊髓拴系松解术的依据。临床上,这些患者表现为新发或近期进展的脊柱侧弯、伴有或不伴有挛缩的痉挛、运动功能减退以及闭合部位的下背部疼痛。所有病例均出现上述一项或多项表现,从而引发对脊髓拴系的怀疑。所有病例均通过MRI或CT脊髓造影确诊为脊髓拴系。为了将拴系确定为患者临床病情恶化的病因,将伴有中枢神经系统并发症(如分流功能障碍或脊髓空洞症)的患者排除在研究之外。最初考虑的59名患者中,有29名基于这一伴有中枢神经系统并发症的标准被排除。术后1年的松解结果如下:关于脊柱侧弯,75%的病例曲线保持稳定或下降超过10度,25%的病例曲线进展超过10度。该组最近的随访显示,11.8%的患者曲率下降超过10度;47.1%保持稳定,41.2%最终进展10度。在痉挛组中,43.8%有所改善;56.3%保持稳定,无病情恶化者。大多数(78.6%)运动功能下降的儿童术后有所改善,所有有背痛的儿童疼痛完全缓解。总之,对有症状的低腰和骶部水平脊髓脊膜膨出儿童进行脊髓拴系松解术似乎有益,特别是对于部分患者脊柱侧弯的稳定、闭合部位的背痛以及先前的运动功能下降。痉挛病例的结果更不明确。