A rare case presentation for congenital pseudarthrosis of collar bone

F. A. Hulaibi, Zainab Mohammed Al Eid, K. Shubair, A. Siddique
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引用次数: 1

Abstract

Congenital pseudarthrosis of the clavicle (CPC) is a rare diagnosis of undetermined etiologies with a limited number of cases were reported. Classically, children patients presenting asymptomatic with a diagnosis that can be confirmed by X-rays with the absence of a central zone portion of the clavicle. Although clinical presentations are variable, which ranges from being asymptomatic to discomfort or sometimes restriction in shoulder range of motion, thus, some cases reported manifestations of thoracic outlet syndromes. Therefore, Management of such cases is individually tailored from conservative to surgical intervention when indicated in overt symptomatic patients or those with significant deformity. Here, we present a case of right-sided CPC in a 13-year-old male patient detected as he concerned about its appearance, which diagnosed and managed non-surgically with further follow- up in our hospital.
先天性锁骨假关节的罕见病例报告
先天性锁骨假关节(CPC)是一种罕见的病因不明的诊断,报告的病例数量有限。传统上,儿童患者表现为无症状,诊断结果可以通过X光片确认,锁骨中心区缺失。尽管临床表现各不相同,从无症状到肩部活动范围不适或有时受限,因此,一些病例报告了胸廓出口综合征的表现。因此,当有明显症状的患者或有严重畸形的患者出现症状时,此类病例的管理是单独定制的,从保守治疗到手术干预。在这里,我们介绍了一例13岁男性患者的右侧CPC,他因担心其外观而被发现,该患者在我们医院进行了非手术诊断和治疗,并进行了进一步的随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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