Ford E G, Jaufmann B A, Kaste S C, Foody L J, Kuivila T E
Department of General Surgery, Scott & White Clinic and Memorial Hospital, Temple, Texas, USA.
J Pediatr Surg. 1996 Jul;31(7):960-4. doi: 10.1016/s0022-3468(96)90422-4.
Congenital segmental spinal dysgenesis is a rare lesion that usually is associated with neurological deficits. Affected infants who are neurologically intact may suffer progressive kyphosis and subsequent neurological deterioration. Results of external casting, laminectomy with spinal fixation, or bone grafting of the defect have been disappointing. The authors present a successful staged surgical management scheme consisting of complete resection of the dysraphic vertebral bodies, maintenance of normal vertebral distance with rib strut grafting, and fusion with autogenous bone.
先天性节段性脊柱发育不全是一种罕见的病变,通常与神经功能缺损相关。神经功能正常的患病婴儿可能会出现进行性驼背及随后的神经功能恶化。外固定支具、椎板切除加脊柱固定或缺损部位植骨的治疗效果均不尽人意。作者提出了一种成功的分期手术治疗方案,包括完全切除脊柱裂椎体、用肋骨支撑植骨维持正常椎体间距以及自体骨融合。