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Surgical treatment of a 180° thoracolumbar fixed kyphosis in a young achondroplastic patient: a one-stage “in situ” combined fusion and spinal cord translocation

机译:一名年轻的软骨发育不全患者的180°胸腰椎固定后凸畸形的外科治疗:一个阶段的“原位”融合和脊髓移位联合治疗

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摘要

An achondroplastic patient with a thoracolumbar kyphosis was first seen at the age of 16 at our institution. His only concern at that time was the aesthetic implication of his deformity. His physical examination was normal except for loss of the neurologic reflexes in the lower limbs. The radiographs showed a fixed 180° thoracolumbar kyphosis with correct frontal and sagittal balances. No spinal cord anomaly was found on MRI. Two years later, he developed a progressive neurogenic claudication of the lower limbs. He was still neurologically intact at rest. The MRI showed an abnormal central spinal cord signal in front of the apex of the kyphosis associated with the narrow congenital spinal canal. In regards to this progressive neurological worsening, a surgical treatment was decided. We decided to perform a front and back arthrodesis combined with a spinal cord decompression without reduction of the deformity. A five-level hemilaminotomy was performed with a posterior approach at the kyphosis deformity. The spinal cord was individualised onto 10 cm and the left nerve roots were isolated. A decancellation osteotomy of the three apex vertebrae and a disc excision were performed. The posterior aspect of the vertebral body was then translated forward 2 cm and in association with the spinal cord. Two nerve roots were severed laterally to approach the anterior part of the kyphosis and a peroneal strut graft was inlayed anterolaterally. A complementary anterior and a right posterolateral fusion was made with cancellous bone. The patient was immobilised in a cast for 3 months relayed by a thoracolumbosacral orthosis for 6 months. At 3 years follow-up, the neurogenic claudication had disappeared. No worsening of the kyphosis was observed. His only complaint is violent electric shock in the lower limbs with any external sudden pressure on the spinal cord in the area uncovered by bone.
机译:首次在我们的机构中​​看到一名患有胸腰椎后凸畸形的软骨发育不全患者,年龄为16岁。当时他唯一关心的是他畸形的美学含义。他的身体检查正常,除了下肢神经反射消失。放射线照片显示固定的180°胸腰椎后凸畸形,具有正确的额叶和矢状位平衡。 MRI未发现脊髓异常。两年后,他发展了下肢进行性神经源性lau行。休息时他仍然神经完好。 MRI显示在与狭窄的先天性椎管相关的后凸畸形的前部,中心脊髓信号异常。关于这种进行性神经学恶化,决定了手术治疗。我们决定在不降低畸形的情况下,进行前,后关节固定结合脊髓减压。对后凸畸形进行后入路五次半切开术。将脊髓个体化到10厘米处,并分离左神经根。进行三个顶点椎骨的去骨截骨术和椎间盘切除术。然后将椎体的后部向前平移2厘米并与脊髓相连。切断两个神经根,使其接近后凸的前部,并在腓骨前外侧镶嵌腓骨支撑物。用松质骨进行互补的前,右后外侧融合。该患者被固定在石膏中3个月,并通过胸腰s骨矫形器进行了6个月的固定。在3年的随访中,神经源性lau行消失了。没有观察到后凸的恶化。他唯一的抱怨是下肢受到剧烈电击,而骨头所覆盖的区域中脊髓受到任何外部突然压力。

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