首页> 外文期刊>The Journal of the American Academy of Orthopaedic Surgeons >Syringomyelia-associated Scoliosis With and Without the Chiari I Malformation.
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Syringomyelia-associated Scoliosis With and Without the Chiari I Malformation.

机译:有和没有Chiari I畸形的脊髓空洞相关脊柱侧弯。

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摘要

Although there may be a hereditary component to true idiopathic scoliosis, the condition has no known cause and is not associated with dysraphism. However, scoliosis with an associated syrinx, with or without the Chiari I malformation, sometimes presents as an idiopathic-type curve. Physical examination findings and subtle clues on diagnostic imaging may help the orthopaedic surgeon diagnose scoliosis associated with syringomyelia. Examination findings include asymmetric reflexes and presentation at ages younger than those of patients who present with adolescent idiopathic curves (ie, 10 to 14 years). Radiologic findings include kyphosis at the apex of the curve. Indications for surgical decompression include progressive neurologic deficits, weakness, pain, and progressive curves. Most orthopaedic surgeons agree that a syrinx should be evaluated neurosurgically before any planned spinal arthrodesis to decrease the risk of neurologic injury connected with surgical correction. The indications for arthrodesis in these patients compared with those with idiopathic curves are evolving.
机译:尽管可能存在真正的特发性脊柱侧弯的遗传因素,但该病情尚无已知原因,也与发育不良无关。但是,脊柱侧弯伴有相关的syrinx,无论是否伴有Chiari I畸形,有时都表现为特发性曲线。体格检查结果和诊断影像学上的细微线索可能有助于骨科医生诊断脊髓空洞症相关的脊柱侧凸。检查的结果包括比出现青春期特发性弯曲的患者(即10至14岁)年轻的不对称反射和表现。放射学发现包括曲线顶点处的后凸畸形。手术减压的适应症包括进行性神经功能缺损,虚弱,疼痛和进行性弯曲。大多数骨科医生都同意,在进行任何计划的脊柱关节固定术之前,应先通过神经外科手术评估syrinx,以减少与手术矫正相关的神经系统损伤的风险。与具有特发性曲线的患者相比,这些患者的关节固定适应症正在发展。

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