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史密斯-马吉尼斯综合征脊柱侧弯的外科治疗:一例报告

Surgical treatment of scoliosis in Smith-Magenis syndrome: a case report.

作者信息

Tsirikos Athanasios I, Baker Alexander Dl, McClean Claire

机构信息

Scottish National Spine Deformity Centre, Royal Hospital for Sick Children, Sciennes Road, Edinburgh, EH9 1LF, UK.

出版信息

J Med Case Rep. 2010 Jan 28;4:26. doi: 10.1186/1752-1947-4-26.

Abstract

INTRODUCTION

Smith-Magenis syndrome is a rare genetic condition associated with scoliosis in approximately 30% of cases. There is limited information in the literature on the treatment of scoliosis and the surgical outcome in patients with this condition. Characteristic features of the syndrome, such as the presence of congenital heart and renal disease, inherent immunodeficiency, as well as severe behavioural disorders may complicate the surgical treatment of patients.

CASE PRESENTATION

We present the case of an 11-year-old British Caucasian girl with Smith-Magenis syndrome who developed a severe, progressive thoracic and lumbar scoliosis measuring 85 degrees and 80 degrees , respectively. She had no cardiac or renal anomalies. Brace treatment was unsuccessful to prevent deterioration of the scoliosis. Both curves were rigid on supine maximum side-bending and traction radiographs. Our patient underwent a posterior spinal arthrodesis with pedicle screw/hook and rod instrumentation and autologous iliac crest graft, supplemented by allograft bone. She had an uneventful postoperative course other than the development of a small wound dehiscence which required resuturing with no signs of a wound infection. A good correction of both scoliotic curvatures to 45 degrees and 40 degrees and a balanced spine in both the coronal and sagittal planes was achieved. Follow-up to skeletal maturity (4 years post-surgery) showed no loss of deformity correction, no detected pseudarthrosis and a good clinical outcome.

CONCLUSION

Patients with Smith-Magenis syndrome can develop a severe scoliosis that may require surgical treatment. Congenital cardiac and renal disease, immunodeficiency and severe behavioural problems can affect the surgical outcome following spinal arthrodesis and need to be taken into consideration. Our case demonstrates that surgical correction of the deformity can be performed safely on this group of patients, with a good outcome and an uncomplicated postoperative course.

摘要

引言

史密斯-马吉尼斯综合征是一种罕见的遗传性疾病,约30%的病例与脊柱侧弯有关。关于该疾病患者脊柱侧弯的治疗及手术结果,文献中的信息有限。该综合征的特征性表现,如先天性心脏和肾脏疾病、固有免疫缺陷以及严重的行为障碍,可能会使患者的手术治疗复杂化。

病例报告

我们报告一例11岁的英国白种女孩,患有史密斯-马吉尼斯综合征,其胸段和腰段脊柱侧弯严重且呈进行性发展,分别为85度和80度。她没有心脏或肾脏异常。支具治疗未能阻止脊柱侧弯恶化。仰卧位最大侧屈和牵引X线片显示两条曲线均僵硬。我们的患者接受了后路脊柱融合术,采用椎弓根螺钉/钩和棒器械固定,并取自体髂嵴骨移植,辅以同种异体骨。术后过程顺利,仅出现一个小的伤口裂开,需要重新缝合,无伤口感染迹象。两条脊柱侧弯曲线均得到良好矫正,分别为45度和40度,脊柱在冠状面和矢状面均达到平衡。随访至骨骼成熟(术后4年),未发现畸形矫正丢失,未检测到假关节形成,临床结果良好。

结论

史密斯-马吉尼斯综合征患者可出现严重的脊柱侧弯,可能需要手术治疗。先天性心脏和肾脏疾病、免疫缺陷以及严重的行为问题会影响脊柱融合术后的手术结果,需要予以考虑。我们的病例表明,对这组患者进行畸形的手术矫正可以安全进行,且效果良好,术后过程无并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c710/2837667/8989c10f385a/1752-1947-4-26-1.jpg

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