Zarzycki Daniel, Rymarczyk Adrian, Bakalarek Bogdan, Kalicinski Mariusz, Winiarski Aleksander
Jagiellonian University Medical College Department of Pediatric Orthopaedics and Rehabilitation, Zakopane, Poland.
Spine (Phila Pa 1976). 2002 Jan 1;27(1):72-7. doi: 10.1097/00007632-200201010-00017.
The essence of congenital vertebral displacement Type A pathology is a congenital structure defect including a vertebral or intervertebral disc with instant curvature of the spinal canal in the sagittal plane. Clinically this defect assumes the shape of kyphosis or kyphoscoliosis. A retrospective review of 11 patients with this congenital deformity was conducted.
To evaluate the effectiveness of surgical treatment for congenital vertebral displacement, and to establish the optimal operative management.
Nine patients with a mean age of 3.3 years (range, 1.8-5.5 years) underwent surgery. Two patients were treated conservatively. All the patients underwent radiologic investigation, which included radiographs, three-dimensional computed tomography scans, and magnetic resonance imaging scans. The neurologic condition was assessed by clinical neurologic examination and somatosensory-evoked potentials. The following surgical techniques were performed: 13 posterior fusions in situ in eight patients; 4 anterior fusions in situ in four patients, 8 total or partial vertebrectomies with anterior fusion and stabilization using cylindric cage in 6 patients, 3 total or partial vertebrectomies with anterior fusion and stabilization using fibula graft in 3 patients, and 5 posterior fusions with instrumentation in 2 patients. The total mean follow-up period was 5.7 years (range, 2.1-9.9 years).
The mean follow-up period after the last operation was 22 months (range, 2-48 months). The general results observed during the follow-up period were as follows. Deformity stabilization was obtained in six patients, whereas it was still progressive in three patients. In five patients, regression of neurologic deficits was obtained, whereas in patients, it was stable. Progression of neurologic deficits was observed in one patient (paraplegia). Retrospectively, the best clinical results were achieved after extensive decompression of the spinal cord with anterior stabilization of the spine using a cylindric cage or fibula autograft. These procedures were preceded or followed by posterior fusion.
The findings showed that only extensive vertebrectomy and anterior stabilization using a cylindric cage or fibula graft combined in one operative procedure, preceded or followed by posterior fusion, ensures patients against progression of neurologic deficits and deformity of spine.
先天性A型椎体移位病理的本质是一种先天性结构缺陷,包括椎体或椎间盘,同时椎管在矢状面有即刻弯曲。临床上,这种缺陷表现为后凸或后凸侧弯畸形。对11例患有这种先天性畸形的患者进行了回顾性研究。
评估先天性椎体移位手术治疗的有效性,并确定最佳手术管理方法。
9例平均年龄3.3岁(范围1.8 - 5.5岁)的患者接受了手术。2例患者接受保守治疗。所有患者均接受了影像学检查,包括X线片、三维计算机断层扫描和磁共振成像扫描。通过临床神经学检查和体感诱发电位评估神经状况。采用了以下手术技术:8例患者进行了13次后路原位融合;4例患者进行了4次前路原位融合;6例患者进行了8次全椎或部分椎体切除并使用圆柱形椎间融合器进行前路融合和固定;3例患者进行了3次全椎或部分椎体切除并使用腓骨移植进行前路融合和固定;2例患者进行了5次后路融合并使用内固定。总平均随访期为5.7年(范围2.1 - 9.9年)。
最后一次手术后的平均随访期为22个月(范围2 - 48个月)。随访期间观察到的总体结果如下。6例患者畸形得到稳定,而3例患者畸形仍在进展。5例患者神经功能缺损有所恢复,而其他患者神经功能缺损情况稳定。1例患者(截瘫)出现神经功能缺损进展。回顾性分析发现,采用圆柱形椎间融合器或自体腓骨移植进行前路脊柱稳定并同时广泛减压脊髓,在此之前或之后进行后路融合,可取得最佳临床效果。
研究结果表明,只有在一次手术中联合进行广泛的椎体切除并使用圆柱形椎间融合器或腓骨移植进行前路稳定,在此之前或之后进行后路融合,才能确保患者避免神经功能缺损进展和脊柱畸形。