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儿童近端桡骨罕见孤立性骨软骨瘤致慢性桡骨头脱位:一例报告并文献复习

Chronic radial head dislocation caused by a rare solitary osteochondroma of the proximal radius in a child: a case report and review of the literature.

作者信息

Niu Xiao-feng, Yi Jian-hua, Hu Jun, Xiao Liang-bao

机构信息

Department of Upper Extremity Orthopedics, Eastern Hospital of the First Affiliated Hospital, Sun Yat-sen University, Guang Zhou, China.

出版信息

BMC Res Notes. 2015 Apr 8;8:131. doi: 10.1186/s13104-015-1095-y.

Abstract

BACKGROUND

Osteochondroma is the most common benign bone tumor of the upper limbs that occurs during the developmental phase of children. Solitary epiphyseal enchondromas can be usually found in the humeral capitellum, and the proximal ulna of the elbow.

CASE PRESENTATION

Herein, we report the case of a 12-year-old boy of Han ethnicity with a developmental radial head dislocation with a progressive radius deformities, caused by a solitary osteochondroma which originated from the proximal metaphysis of the radius. Obvious complaints and limitations were present. After tumor excision was performed, radial head reduction and deformity correction were achieved through a biplanar shortening osteotomy of the radius.

CONCLUSIONS

After a follow-up of 18 months, the child remained asymptomatic and regained a full range of motion. Radiographic study revealed satisfactory reduction of the radial head with no recurrence of the osteochondroma.

摘要

背景

骨软骨瘤是儿童发育阶段上肢最常见的良性骨肿瘤。孤立性骨骺内生软骨瘤通常见于肱骨小头和肘部尺骨近端。

病例介绍

在此,我们报告一例12岁汉族男孩,因起源于桡骨近端干骺端的孤立性骨软骨瘤导致发育性桡骨头脱位及桡骨渐进性畸形。存在明显的症状和功能受限。肿瘤切除后,通过桡骨双平面缩短截骨术实现了桡骨头复位和畸形矫正。

结论

随访18个月后,患儿无症状,恢复了全范围活动。影像学检查显示桡骨头复位满意,骨软骨瘤无复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5b6/4393608/d9771927f8b3/13104_2015_1095_Fig1_HTML.jpg

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