Severe aortic valve regurgitation in patient with Takayasu arteritis: a case report.

Pub Date : 2024-09-04 eCollection Date: 2024-09-01 DOI:10.1093/ehjcr/ytae473
Vasiliki Tassi, Dimitrios Tzalas, Elektra Papadopoulou, Athanasios Trikas
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Abstract

Background: Takayasu arteritis (TAK) is a systemic non-inflammatory vasculitis that primarily affects large- and medium-sized arteries.

Case summary: We report the case of a 57-year-old woman with a history of coronary artery bypass grafting (CABG) 7 years prior, who was referred for a stress echo due to chest pain. Transthoracic echocardiography revealed the left ventricle at the upper limits of normal with preserved contractility, as well as circumferential thickening of the aortic root, causing severe aortic regurgitation (AR). Cardiac computed tomography and angiography demonstrated diffuse thickening of the aortic wall from the aortic root to the descending thoracic aorta, extending to the left carotid artery and significant stenosis of the left subclavian artery. Coronary angiography showed severe narrowing of the left main coronary ostium with ostial stenosis and total occlusion of the right coronary and left internal mammary arteries. Magnetic angiography highlighted thickening of the aortic wall, while no active inflammation was detected on positron emission tomography. These findings suggested Takayasu aortitis with chronic inflammation.

Discussion: In young patients, particularly women, who present with angina and coronary ostial stenosis, Takayasu arteritis should be considered in the differential diagnosis. Aortic regurgitation (AR) is a serious complication, and its surgical management can be challenging.

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高安动脉炎患者的严重主动脉瓣反流:病例报告。
背景:病例摘要:我们报告了一例 57 岁女性患者的病例,该患者 7 年前接受过冠状动脉旁路移植术(CABG),因胸痛转诊接受压力回波检查。经胸超声心动图显示左心室处于正常上限,收缩力保留,主动脉根部周缘增厚,导致严重的主动脉瓣反流(AR)。心脏计算机断层扫描和血管造影显示,从主动脉根部到降胸主动脉的主动脉壁弥漫性增厚,并延伸至左颈动脉,左锁骨下动脉明显狭窄。冠状动脉造影显示,左冠状动脉主干骨膜严重狭窄,骨膜狭窄,右冠状动脉和左乳内动脉完全闭塞。磁性血管造影显示主动脉壁增厚,而正电子发射断层扫描没有发现活动性炎症。这些结果表明高安主动脉炎伴有慢性炎症:讨论:对于出现心绞痛和冠状动脉口狭窄的年轻患者,尤其是女性患者,在鉴别诊断时应考虑高安市动脉炎。主动脉瓣反流(AR)是一种严重的并发症,其手术治疗具有挑战性。
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