A case of Takayasu arteritis with normal coronary arteries presenting as stable angina

S. A. P. N. Samarasingha, A. Kirubaharan, J. A. Vasanthan, H. Jayawardena, W. A. Jayanaga
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Abstract

Takayasu arteritis (TAK) is a type of large vessel vasculitis characterized by granulomatous inflammation involving the aorta and its main branches. Clinical presentation may vary from non specific symptoms such as fever, malaise, weight loss to manifestations of organ hypo perfusion. Cardiac involvement may take forms of valvular insufficiency, angina or heart failure. In this case, we report a 39-year-old woman with hypertension presenting with angina, who was found to have multiple arterial bruits, with blood pressure and pulse volume discrepancies, aortic regurgitation and renovascular hypertension. She was diagnosed with Takayasu arteritis with clinical and imaging criteria; managed with glucocorticoid and DMARDS, achieving good clinical response and planned for surgical intervention for valvular insufficiency.
一例冠状动脉正常但表现为稳定型心绞痛的高安动脉炎患者
高安动脉炎(TAK)是一种大血管炎,其特征是累及主动脉及其主要分支的肉芽肿性炎症。临床表现多种多样,从发热、乏力、体重减轻等非特异性症状到器官灌注不足的表现。心脏受累可表现为瓣膜功能不全、心绞痛或心力衰竭。在本病例中,我们报告了一名 39 岁的女性高血压患者,她出现心绞痛,被发现有多处动脉淤血,血压和脉搏量不一致,主动脉瓣反流和新血管性高血压。根据临床和影像学标准,她被诊断为高安动脉炎;使用糖皮质激素和 DMARDS 进行治疗,取得了良好的临床反应,并计划进行外科手术治疗瓣膜功能不全。
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