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作 者:鄢飞[1] 寿康全 鲍同柱[1] 王河洲[1] Yan Fei;Shou Kangquan;Bao Tongzhu;Wang Hezhou(Department of Orthopaedics,Yichang Central People's Hospital,The First College of Clinical Medical Science,China Three Gorges University,Yichang 443003,China)
机构地区:[1]三峡大学第一临床医学院[宜昌市中心人民医院]骨科,湖北宜昌443003
出 处:《巴楚医学》2024年第4期38-40,共3页Bachu Medical Journal
基 金:湖北省自然科学基金项目(No:2021CFB488)。
摘 要:先天性锁骨假关节(CPC)是一种罕见疾病,发病机制倾向于“胚胎学”论,即两个锁骨骨化中心融合失败所致。临床表现为无痛性包块,易误诊为肿瘤或锁骨骨折后骨不连,甚至误认为产伤所致。本文详细介绍一例双侧CPC患者的诊疗过程,结合最新文献,讨论CPC的鉴别诊断、手术指征及手术方式,旨在为临床医生在诊治此类疾病时提供经验参考。Congenital pseudoarthrosis of clavicle(CPC)is a rare disease,and the pathogenesis tends to be the“embryological”theory,that is,the failure of the fusion of the two ossification centers of the clavicle.The clinical manifestation is painless mass,which is easily misdiagnosed as tumor or bone union after clavicle fracture,and even mistaken as caused by labor injury.This paper introduces in detail the diagnosis and treatment process of a bilateral CPC patient and discusses the differential diagnosis,surgical indication and surgical methods of CPC combined with the latest literature,aiming to provide experience reference for clinicians in the diagnosis and treatment of this disease.
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