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先天性尺桡骨融合

Congenital Radioulnar Synostosis.

机构信息

From the Department of Orthopaedics, Mount Carmel Health System, Columbus, OH (Rutkowski), and the Department of Orthopedic Surgery, Nationwide Children's Hospital, Columbus, OH (Samora).

出版信息

J Am Acad Orthop Surg. 2021 Jul 1;29(13):563-570. doi: 10.5435/JAAOS-D-20-01133.

Abstract

Congenital radioulnar synostosis is a rare condition resulting in fusion of the proximal portions of the radius and ulna. Patients commonly present in early childhood with functional deficits because of limited forearm rotation and fixed positioning of the forearm. Compensatory motion and hypermobility are frequently observed at the wrist and shoulder, which may predispose these joints to overuse injury. Plain radiographs are used for diagnosis and classification. The most commonly used classification does not aid in treatment decisions. Limited high-level evidence exists to guide management because the literature primarily consists of case reports and case series. Nonsurgical management is often used, yet surgical management is most commonly reported in the literature. Resection of the synostosis has been shown to have high-complication rates and lead to subpar outcomes. Currently, surgical management most commonly involves one or more derotational osteotomies.

摘要

先天性桡尺骨融合是一种罕见的疾病,导致桡骨和尺骨近端融合。由于前臂旋转受限和前臂固定位置,患者通常在幼儿期出现功能缺陷。腕关节和肩关节经常出现代偿性运动和过度活动,这可能使这些关节容易发生过度使用损伤。平片用于诊断和分类。最常用的分类方法并不能帮助治疗决策。由于文献主要由病例报告和病例系列组成,因此仅有有限的高级别证据可用于指导管理。非手术治疗通常用于治疗,但手术治疗在文献中最常被报道。融合切除已被证明具有高并发症发生率,并导致结果不佳。目前,手术治疗最常见的方法是进行一次或多次旋转截骨术。

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