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首页> 外文期刊>Journal of neurosurgery. >Spinal stenosis surgery in pediatric patients with achondroplasia.
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Spinal stenosis surgery in pediatric patients with achondroplasia.

机译:小儿软骨发育不全的椎管狭窄手术。

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OBJECT: Achondroplasia is a hereditary form of dwarfism caused by a defect in endochondral bone formation, resulting in skeletal abnormalities including short stature, shortened limb bones, macrocephaly, and small vertebral bodies. In the pediatric population, symptomatic spinal stenosis occurs at all spinal levels due to the abnormally narrow bone canal. In this study, clinical outcomes were assessed in children with achondroplasia after spinal canal decompression. METHODS: A retrospective review was conducted involving pediatric patients with heterozygous achondroplasia and symptomatic stenosis after decompressive procedures at the authors' institution within a 9-year period. Measured outcomes included resolution of symptoms, need for repeated surgery, presence of fusion, development of deformity, and complications. Forty-four pediatric patients underwent a total of 60 decompressive procedures. The average patient age at surgery was 12.7 years (range 5-21 years). Forty-nine operations were performed for initial treatment of stenosis, and 11 were performed as revision surgeries on previously operated levels. A large proportion of patients (> 60%) required additional cervicomedullary decompressions, most often preceding the symptoms of spinal stenosis. Of the initial procedures, decompression locations included 32 thoracolumbar (65%), 10 lumbar (20%), four cervical (8%), two cervicothoracic (4%), and one thoracic (2%). Forty-three of the decompressive procedures (72%) included spinal fusion procedures. Of the 11 revisions, five were fusion procedures for progressive deformity at levels previously decompressed but not fused (all thoracolumbar), five were for decompressions of symptomatic junctional stenosis with extension of fusion, and one was for repeated decompression at the same level due to recurrence of symptomatic stenosis. CONCLUSIONS: Decompression of the spinal canal in pediatric patients with achondroplasia can be accomplished safely with significant clinical benefit. Patients with a history of cervicomedullary compression may be at an increased risk of developing symptomatic stenosis prior to adolescence. Fusion procedures are recommended in patients with a large decompression overlying a thoracolumbar kyphosis to avoid progressive postoperative deformity.
机译:目的:软骨病是一种侏儒症的遗传形式,由软骨内骨形成缺陷引起,导致骨骼异常,包括身材矮小,四肢短,大头畸形和小椎体。在小儿人群中,由于异常狭窄的骨管,在所有脊柱水平上都会出现有症状的脊椎狭窄。在这项研究中,对椎管减压后儿童软骨发育不全的儿童评估了临床结局。方法:在作者机构进行的为期9年的减压手术后,对患有杂合性软骨发育不良和症状性狭窄的小儿患者进行了回顾性研究。测量的结果包括症状的缓解,是否需要重复手术,是否存在融合,畸形的发展以及并发症。四十四名儿科患者总共接受了60次减压手术。手术时的平均患者年龄为12.7岁(5-21岁)。对狭窄的初始治疗进行了49例手术,在以前的手术水平上进行了11例作为翻修手术。很大一部分患者(> 60%)需要额外的子宫颈髓腔减压,最常出现脊椎狭窄的症状。在最初的手术中,减压部位包括32个胸腰椎(65%),10个腰椎(20%),4个颈椎(8%),2个颈胸腔酸(4%)和1个胸腔(2%)。 43例减压手术(占72%)包括脊柱融合手术。在11个修订版中,有5个是融合手术,用于进行先前减压但未融合的水平的进行性畸形(全部胸腰椎),有5个是对有症状的结节狭窄减压并融合的延长,另一个是因复发而在相同水平重复减压有症状的狭窄。结论:小儿软骨发育不良患者的椎管减压可以安全地完成,并具有明显的临床益处。有子宫颈髓核压迫病史的患者,在青春期之前出现症状性狭窄的风险可能会增加。对于有较大减压的胸腰椎后凸畸形患者,建议进行融合手术,以避免术后进行性畸形。

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