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罕见疾病脊柱侧弯的手术治疗:先天性多发性关节挛缩症

Surgical treatment of scoliosis in a rare disease: arthrogryposis.

作者信息

Greggi Tiziana, Martikos Konstantinos, Pipitone Emanuela, Lolli Francesco, Vommaro Francesco, Maredi Elena, Cervellati Stefano, Silvestre Mario Di

机构信息

Spine Surgery Division, Rizzoli Orthopaedic Institute, Bologna, Italy.

出版信息

Scoliosis. 2010 Nov 9;5:24. doi: 10.1186/1748-7161-5-24.

Abstract

BACKGROUND

The reported incidence of scoliosis in arthrogryposis varies from 30% to 67% and, in most cases, the curves progress rapidly and become stiff from early age.The authors report six cases of scoliosis in arthrogryposis to assess the role of surgical treatment.

METHODS

Six cases (3 males, 3 females; mean age at surgery 13.2 years) with arthrogryposis multiplex congenita associated with the characteristic amyoplasia were reviewed: they were operated on for scoliosis at the authors' Spine Surgery Department between 1987 and 2008.Surgery was performed using the Harrington-Luque instrumentation (2 cases), the Luque system (1), a hybrid segmental technique with hooks and screws (1) and spinal anchoring with pedicle screws (2).

RESULTS

The patients were clinically and radiologically reviewed at a mean follow-up of 4.2 years, ± 2.7 (range, 1 to 9 years). Three minor postoperative complications were encountered; a long-term pulmonary complication was seen in one case after reintervention and was successfully resolved after 10 days. Surgery was successful in the other 5 cases, where solid arthrodesis was achieved and no significant curve progression was observed at follow-up.

CONCLUSIONS

The experience acquired with the present case series leads the authors to assert that prompt action should be taken when treating such aggressive forms of scoliosis. In case of mild spinal deformities in arthrogryposis, brace treatment should be attempted, the evolution of the curves being unpredictable; however, when the curve exceeds 40° and presents with marked hyperkyphosis, hyperlordosis or pelvic obliquity, surgery should not be delayed.

摘要

背景

关节挛缩症中脊柱侧弯的报道发病率在30%至67%之间,在大多数情况下,侧弯曲线从幼年起就迅速进展并变得僵硬。作者报告6例关节挛缩症合并脊柱侧弯病例,以评估手术治疗的作用。

方法

回顾6例(3男,3女;手术时平均年龄13.2岁)患有先天性多发性关节挛缩症并伴有典型的肢体肌肉发育不全的病例:1987年至2008年间,他们在作者所在的脊柱外科接受了脊柱侧弯手术。手术采用哈灵顿-卢克器械(2例)、卢克系统(1例)、钩和螺钉混合节段技术(1例)以及椎弓根螺钉脊柱内固定(2例)。

结果

平均随访4.2年±2.7年(范围1至9年),对患者进行了临床和影像学检查。出现了3例轻微术后并发症;1例再次干预后出现长期肺部并发症,10天后成功解决。其他5例手术成功,实现了坚固的脊柱融合,随访时未观察到侧弯曲线明显进展。

结论

通过本病例系列获得的经验使作者断言,治疗这种侵袭性脊柱侧弯时应迅速采取行动。对于关节挛缩症合并轻度脊柱畸形的情况,应尝试支具治疗,因为侧弯曲线的演变不可预测;然而,当侧弯超过40°并伴有明显的后凸、前凸或骨盆倾斜时,不应延迟手术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ab7/2991290/afe0f21822b5/1748-7161-5-24-1.jpg

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