Winter R B, Moe J H, Bradford D S, Lonstein J E, Pedras C V, Weber A H
J Bone Joint Surg Am. 1979 Jul;61(5):677-94.
The natural history, associated anomalies, and response to operative and nonoperative treatment were reviewed in 102 patients with neurofibromatosis and spine deformity. Eighty patients were found to have curvatures associated with dystrophic changes in the vertebrae and ribs. The presence of dystrophic changes such as rib penciling, spindling of the transverse processes, vertebral scalloping, severe apical vertebral rotation, foraminal enlargement, and adjacent soft-tissue neurofibromas was found to be highly significant in prognosis and management. Brace treatment of dystrophic curves was unsuccessful. Posterior fusion, with or without internal fixation, was the procedure of choice for problems due purely to scoliosis. Patients with dystrophic kyphoscoliosis required both anterior and posterior fusion to achieve stability. Sixteen patients had compression of the spinal cord or cauda equina.
对102例患有神经纤维瘤病和脊柱畸形的患者的自然病史、相关异常情况以及手术和非手术治疗的反应进行了回顾。发现80例患者的脊柱侧弯与椎骨和肋骨的营养不良性改变有关。肋骨铅笔样征、横突纺锤样变、椎体扇贝样变、严重的顶椎旋转、椎间孔扩大以及相邻软组织神经纤维瘤等营养不良性改变的存在,在预后和治疗方面具有高度显著性。对营养不良性脊柱侧弯进行支具治疗未获成功。单纯因脊柱侧凸问题,后路融合术,无论有无内固定,都是首选的手术方式。患有营养不良性脊柱后凸侧弯的患者需要前后路联合融合以实现稳定。16例患者存在脊髓或马尾神经受压情况。