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索托斯综合征(脑性巨人症)患者的脊柱畸形。

Spinal deformity in patients with Sotos syndrome (cerebral gigantism).

作者信息

Tsirikos Athanasios I, Demosthenous Nestor, McMaster Michael J

机构信息

Scottish National Spine Deformity Center, Royal Hospital for Sick Children, Edinburgh, UK.

出版信息

J Spinal Disord Tech. 2009 Apr;22(2):149-53. doi: 10.1097/BSD.0b013e318167b0a6.

Abstract

STUDY DESIGN

Retrospective review of a case series.

OBJECTIVE

To present the clinical characteristics and progression of spinal deformity in patients with Sotos syndrome.

SUMMARY OF BACKGROUND DATA

There is limited information on the development of spinal deformity and the need for treatment in this condition.

METHODS

The medical records and spinal radiographs of 5 consecutive patients were reviewed. All patients were followed to skeletal maturity (mean follow-up: 6.6 y).

RESULTS

The mean age at diagnosis of spinal deformity was 11.9 years (range: 5.8 to 14.5) with 4 patients presenting in adolescence. The type of deformity was not uniform. Two patients presented in adolescence with relatively small and nonprogressive thoracolumbar and lumbar scoliosis, which required observation but no treatment until the end of spinal growth. Three patients underwent spinal deformity correction at a mean age of 11.7 years (range: 6 to 15.4). The first patient developed a double structural thoracic and lumbar scoliosis and underwent a posterior spinal arthrodesis extending from T3 to L4. Five years later, she developed marked degenerative changes at the L4/L5 level causing symptomatic bilateral lateral recess stenosis and affecting the L5 nerve roots. She underwent spinal decompression at L4/L5 and L5/S1 levels followed by extension of the fusion to the sacrum. The second patient developed a severe thoracic kyphosis and underwent a posterior spinal arthrodesis. The remaining patient presented at the age of 5.9 years with a severe thoracic kyphoscoliosis and underwent a 2-stage antero-posterior spinal arthrodesis.

CONCLUSIONS

The development of spinal deformity is a common finding in children with Sotos syndrome and in our series it occurred in adolescence in 4 out of 5 patients. There is significant variability on the pattern of spine deformity, ranging from a scoliosis through kyphoscoliosis to a pure kyphosis, and also the age at presentation and need for treatment.

摘要

研究设计

对一组病例进行回顾性研究。

目的

阐述索托斯综合征患者脊柱畸形的临床特征及进展情况。

背景资料总结

关于这种情况下脊柱畸形的发展及治疗需求的信息有限。

方法

回顾了连续5例患者的病历和脊柱X线片。所有患者均随访至骨骼成熟(平均随访时间:6.6年)。

结果

脊柱畸形诊断时的平均年龄为11.9岁(范围:5.8至14.5岁),其中4例患者在青春期出现畸形。畸形类型并不一致。2例青春期患者出现相对较小且无进展的胸腰段和腰椎脊柱侧凸,在脊柱生长结束前只需观察,无需治疗。3例患者平均在11.7岁(范围:6至15.4岁)时接受了脊柱畸形矫正。第一例患者出现双结构性胸腰段脊柱侧凸,接受了从T3至L4的后路脊柱融合术。5年后,她在L4/L5水平出现明显的退行性改变,导致有症状的双侧侧隐窝狭窄并影响L5神经根。她在L4/L5和L5/S1水平接受了脊柱减压术,随后将融合范围扩展至骶骨。第二例患者出现严重的胸椎后凸畸形,接受了后路脊柱融合术。其余患者在5.9岁时出现严重的胸段脊柱后凸侧凸畸形,接受了两阶段的前后路脊柱融合术。

结论

脊柱畸形在索托斯综合征患儿中很常见,在我们的系列研究中,5例患者中有4例在青春期出现脊柱畸形。脊柱畸形的模式差异很大,从脊柱侧凸到脊柱后凸侧凸再到单纯的后凸畸形,以及出现畸形的年龄和治疗需求都有所不同。

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