Kelley Brian J, Johnson Michele H, Vortmeyer Alexander O, Smith Brian G, Abbed Khalid M
Yale Spine Institute, Department of Neurosurgery, Yale University School of Medicine, New Haven, Connecticut 06520-8082, USA.
J Neurosurg Pediatr. 2012 Oct;10(4):334-9. doi: 10.3171/2012.7.PEDS11526. Epub 2012 Aug 3.
The authors report a case in which multilevel thoracic pedicle subtraction osteotomy (PSO) was performed to correct post-laminectomy kyphotic deformity in a 9-year-old boy presenting with worsening lower-extremity neurological deficits. Five years prior to presentation, the patient underwent multilevel thoracolumbar laminectomies for resection of an atypical teratoid/rhabdoid tumor (AT/RT), a rare lesion that typically occurs intracranially and has a poor prognosis, making this particular presentation unusual and the patient's subsequent postoperative course remarkable. No fusion was undertaken at the time of resection, given the patient's age and presumptive poor prognosis. Over the next 5 years, the patient developed progressive thoracolumbar kyphotic deformity, with a Cobb angle greater than 110°, despite bracing, and bilateral lower-extremity weakness requiring ankle-foot orthotics for continued ambulation due to progressive foot drop. Worsening gait and the onset of respiratory issues prompted surgical intervention. Multilevel thoracic PSO and thoracolumbar fusion were performed, resulting in improved lower-extremity function and correction of the kyphotic deformity to approximately 65°. This report outlines an unusual AT/RT presentation and postoperative course and also discusses literature related to PSO within the context of pediatric kyphotic deformity. The authors' experience supports the use of multilevel PSO with fusion as a potential treatment option for significant pediatric thoracolumbar kyphotic deformity requiring surgical correction.
作者报告了一例病例,该病例为一名9岁男孩,因下肢神经功能缺损恶化,接受了多级胸椎椎弓根截骨术(PSO)以纠正椎板切除术后的脊柱后凸畸形。在出现症状的五年前,该患者接受了多级胸腰椎椎板切除术,以切除一个非典型畸胎样/横纹肌样瘤(AT/RT),这是一种罕见的病变,通常发生在颅内,预后较差,使得这一特殊病例不同寻常,患者随后的术后病程也引人注目。鉴于患者年龄和预期的不良预后,在切除肿瘤时未进行融合手术。在接下来的5年里,尽管进行了支具治疗,但患者仍逐渐发展为胸腰椎脊柱后凸畸形,Cobb角大于110°,并且出现双侧下肢无力,由于进行性足下垂,需要佩戴踝足矫形器才能继续行走。步态恶化和呼吸问题的出现促使进行手术干预。实施了多级胸椎PSO和胸腰椎融合术,结果下肢功能得到改善,脊柱后凸畸形矫正至约65°。本报告概述了一例不寻常的AT/RT病例及其术后病程,并在小儿脊柱后凸畸形的背景下讨论了与PSO相关的文献。作者的经验支持将多级PSO联合融合术作为需要手术矫正的严重小儿胸腰椎脊柱后凸畸形的一种潜在治疗选择。