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一名患有遗传性多发性骨软骨瘤的儿童髋关节进行性半脱位。

Progressive subluxation of the hip joint in a child with hereditary multiple exostosis.

作者信息

Ofiram Elisha, Porat Shlomo

机构信息

Orthopedic Surgery Department, The Hadassah-Hebrew University Medical School, Jerusalem, Israel.

出版信息

J Pediatr Orthop B. 2004 Nov;13(6):371-3. doi: 10.1097/01202412-200411000-00004.

Abstract

We describe the treatment and follow-up of a case of hereditary multiple exostosis in a 16-year-old girl, who had intraarticular and extraarticular osteochondromas in the right hip joint which caused hip subluxation. These osteochondromas were excised, the femoral head was located concentrically, and the patient was put in a spica cast for 6 weeks. Six months later, hip magnetic resonance imaging showed no evidence of avascular necrosis. Three years after the operation the patient walked freely, without pain, and there was satisfying coverage of the femoral head. The authors emphasize that careful attention should be given to the surgical technique prior to extraarticular and intraarticular acetabular osteochondroma excision in order to avoid the development of avascular necrosis.

摘要

我们描述了一名16岁女孩遗传性多发性外生骨疣病例的治疗及随访情况,该女孩右髋关节存在关节内和关节外骨软骨瘤,导致髋关节半脱位。切除了这些骨软骨瘤,使股骨头同心复位,患者髋人字石膏固定6周。6个月后,髋关节磁共振成像显示无缺血性坏死迹象。术后3年,患者行走自如,无疼痛,股骨头覆盖良好。作者强调,在切除关节外和关节内髋臼骨软骨瘤之前,应仔细关注手术技术,以避免缺血性坏死的发生。

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