Suppr超能文献

先天性挛缩性蜘蛛指(趾)畸形的临床诊断与外科治疗:附6例分析

[Clinical diagnosis and surgical treatment of congenital contractural arachnodactyly: analysis of 6 cases].

作者信息

Wang Xue-song, Zhang Jian-guo, Qiu Gui-xing, Weng Xi-sheng, Gao Zeng-xin, Lu Wen-can, Zhao Li-juan

机构信息

Department of Orthopedics, Peking Union medical College Hospital, Peking Union Medical College, Beijing 100730, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2008 Mar 4;88(9):615-8.

Abstract

OBJECTIVE

To discuss the clinical diagnosis and surgical treatment of congenital contractural arachnodactyly (CCA).

METHODS

The clinical data of 6 CCA patients, 1 male and 5 female, aged 7.5 (5-14) were analyzed. All cases had kyphoscoliosis, 2 in the thoracic segments and 4 in the thoracolumbar segments. The average scoliosis Cobb angle was 88.6 degrees (85 degrees-117 degrees). The average kyphosis Cobb angle was 93.6 degrees (75 degrees-123 degrees). All of the cases underwent internal fixation with pedicle screw and lamina hooks instrumentation, in which 4 cases underwent posterior Smith-Petersen osteotomy. The diagnosis was based on a constellation of clinical findings. The clinical manifestations included marfanoid habitus, flexion contractures of multiple joints (elbow, knee, hip, and finger), kyphoscoliosis, muscular hypoplasia, and abnormal pinnae ("crumpled" outer helices). Molecular genetic testing showed mutation in the fibrillin-2 (FBN2) gene encoding the extracellular matrix microfibril. Four cases were followed up for 6-9 months.

RESULTS

After operation the average Cobb angle of the scoliosis and kyphosis were 37.6 degrees (35 degrees-52 degrees) and 38.6 degrees (28 degrees-54 degrees) immediately, with 62.3% and 68.7% curve correction respectively. Three cases got excellent synostosis of posterior lamina, 1 case underwent revision with lamina hook because the distal screw was loose and hurt the nerve root, and the other 2 cases lost follow-up. The patients' body appearance and pulmonary function were obviously improved.

CONCLUSION

The characteristic clinical manifestation include severe and stiff kyphoscoliosis, difficult to correct , and enhanced Cobb angle, and pedicle dysplasia of vertebral pedicle leading to difficulty in installing screws. Smith-Petersen osteotomy is often necessary. CCA should be differentiated with Marfan syndrome (MFS), Stickler syndrome, Homocystinuria, and distal arthrogryposis, especially MFS.

摘要

目的

探讨先天性挛缩性蜘蛛指(趾)症(CCA)的临床诊断及外科治疗方法。

方法

分析6例CCA患者的临床资料,其中男性1例,女性5例,年龄7.5岁(5 - 14岁)。所有病例均有脊柱侧弯,其中胸段2例,胸腰段4例。脊柱侧弯Cobb角平均为88.6度(85度 - 117度)。后凸Cobb角平均为93.6度(75度 - 123度)。所有病例均采用椎弓根螺钉和椎板钩内固定术,其中4例行后路Smith-Petersen截骨术。诊断依据一系列临床发现。临床表现包括类马凡体型、多关节(肘、膝、髋和手指)屈曲挛缩、脊柱侧弯后凸、肌肉发育不全及耳廓异常(“皱缩”的外耳轮)。分子遗传学检测显示编码细胞外基质微原纤维的原纤蛋白-2(FBN2)基因发生突变。4例患者随访6 - 9个月。

结果

术后脊柱侧弯和后凸的Cobb角立即平均分别为37.6度(35度 - 52度)和38.6度(28度 - 54度),曲线矫正分别为62.3%和68.7%。3例后路椎板融合良好,1例因远端螺钉松动损伤神经根而行椎板钩翻修术,另外2例失访。患者的外观及肺功能明显改善。

结论

CCA的特征性临床表现为严重且僵硬的脊柱侧弯后凸、难以矫正、Cobb角增大以及椎弓根发育异常导致螺钉置入困难。常需行Smith-Petersen截骨术。CCA应与马凡综合征(MFS)、Stickler综合征、同型胱氨酸尿症及远端关节挛缩症相鉴别,尤其是MFS。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验