Takayasu arteritis miss-diagnosed as thoracic outlet syndrome: A case report

Naseh Yousefi, P. Roomizadeh, G. Raissi, S. Sadeghi, Katayoun Moradi, Shahram Rahimi-Dehgolan
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Abstract

Background: Takayasu Arteritis (TA) is an idiopathic inflammatory vasculitis of unknown etiology that mainly involves the aorta and its major branches. In this study, we reported the case of a female patient with unilateral hand weakness that was initially misdiagnosed as TOS. However, at her most recent admission, the absence of radial pulse was noted which eventually led to the diagnosis of TA. Rarity of the disease, non-specific presentation and the absence of specific biochemical marker for TA made its early diagnosis difficult. We have tried to highlight the importance of conducting a thorough the physical examination when visiting patients with weakness, as well as the importance of considering rare differential diagnoses including TA in patients with unilateral limb paresis. TA might not manifest its typical constitutional symptoms preceding vessel involvement. Therefore, a thorough clinical examination is pivotal in differentiating TA and TOS.
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高须动脉炎误诊为胸廓出口综合征1例
背景:高松动脉炎(Takayasu Arteritis, TA)是一种病因不明的特发性炎症性血管炎,主要累及主动脉及其主要分支。在本研究中,我们报告了一例女性患者单侧手部无力,最初被误诊为TOS。然而,在她最近一次入院时,发现桡动脉脉搏消失,最终诊断为TA。罕见的疾病,非特异性表现和缺乏特异性生化标志物的TA使其早期诊断困难。我们试图强调在访问虚弱患者时进行彻底的身体检查的重要性,以及在单侧肢体轻瘫患者中考虑包括TA在内的罕见鉴别诊断的重要性。TA可能没有血管受累前的典型体质症状。因此,彻底的临床检查是鉴别TA和TOS的关键。
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