先天性桡尺骨融合——病例报告
Congenital radioulnar synostosis - case report.
作者信息
Siemianowicz Anna, Wawrzynek Wojciech, Besler Krzysztof
机构信息
Department of Diagnostic Imaging, District Hospital of Orthopedics and Trauma Surgery, Piekary Śląskie, Poland.
出版信息
Pol J Radiol. 2010 Oct;75(4):51-4.
BACKGROUND
Congenital radioulnar synostosis is a rare malformation of the upper limb, with functional limitations of the limb.
CASE REPORT
A 10-year-old child with pain and restricted mobility of the elbow joint was admitted to the hospital. Plain film radiography and CT examination was performed. Radiological examinations showed a congenital radioulnar synostosis. The child underwent surgical treatment - derotational osteotomy.
CONCLUSIONS
Diagnostic imaging including computed tomography with three-dimentional (3D) reconstructions, preceding surgery enables planning of the surgical treatment.
背景
先天性桡尺骨融合是一种罕见的上肢畸形，会导致肢体功能受限。
病例报告
一名10岁儿童因肘关节疼痛和活动受限入院。进行了X线平片和CT检查。影像学检查显示为先天性桡尺骨融合。该患儿接受了手术治疗——旋转截骨术。
结论
手术前进行包括三维（3D）重建的计算机断层扫描等诊断性成像，有助于规划手术治疗方案。
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