Lao Lifeng, Zhong Guibin, Li Xinfeng, Liu Zude
Department of Orthopedic Surgery, Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Pediatr Neurosurg. 2013;49(2):69-74. doi: 10.1159/000356890. Epub 2014 Jan 9.
Split spinal cord malformation (SSCM) is rare in scoliosis. This study evaluated the safety and effectiveness of one-stage surgical treatment of congenital scoliosis (CS) in patients with SSCM in a single Chinese center.
A retrospective study of 5 cases who underwent surgery for CS with SSCM (2 type I and 3 type II) from March 2004 to March 2012. Patients included 4 females and 1 male with a mean age of 13.8 years. All patients underwent one-stage posterior fusion surgery with resection of a bony spur firstly in SSCM type I, but we did nothing to the SSCM in type II. Clinical symptoms and radiological changes were evaluated preoperatively and for at least 2 years postoperatively.
Preoperatively, 5 patients had variant neurological and other symptoms. They had a mean preoperative Cobb angle of 63 ± 20° and T5-T12 kyphosis of 30 ± 21°. The mean postoperative Cobb angle was 30.2 ± 19.8° with a correction rate of 57.2 ± 17.0%. At the 3-month follow-up the Cobb angle loss was 3.0 ± 6.8°, and at the 2-year follow-up the Cobb angle loss was 6.5 ± 9.7°. Hyperkyphosis was significantly corrected after surgery but correction loss was indicated at the 2-year follow-up (p < 0.01). There were no neurological deficit complications or deteriorated neurological signs postoperatively or at follow-up.
One-stage surgical treatment of CS with SSCM could be safe and effective, but we need further multicenter studies with larger samples. Intraspinal intervention of bone spur was recommended in SSCM type I before deformity correction, while in SSCM type II it was needless.
脊髓纵裂畸形(SSCM)在脊柱侧弯中较为罕见。本研究评估了在中国单一中心对患有SSCM的先天性脊柱侧弯(CS)患者进行一期手术治疗的安全性和有效性。
对2004年3月至2012年3月期间接受CS合并SSCM手术(2例I型和3例II型)的5例患者进行回顾性研究。患者包括4名女性和1名男性,平均年龄13.8岁。所有患者均接受一期后路融合手术,I型SSCM患者首先切除骨赘,但II型SSCM患者未对其进行处理。术前及术后至少2年评估临床症状和影像学变化。
术前,5例患者有不同的神经及其他症状。术前平均Cobb角为63±20°,T5 - T12后凸角为30±21°。术后平均Cobb角为30.2±19.8°,矫正率为57.2±17.0%。3个月随访时Cobb角丢失为3.0±6.8°,2年随访时Cobb角丢失为6.5±9.7°。术后后凸畸形得到显著矫正,但在2年随访时有矫正丢失(p<0.01)。术后及随访期间均无神经功能缺损并发症或神经体征恶化。
CS合并SSCM的一期手术治疗可能是安全有效的,但我们需要进一步开展更大样本量的多中心研究。对于I型SSCM,建议在矫正畸形前对骨赘进行椎管内干预,而II型SSCM则无需干预。