Unveiling the Silent Constrictor: A Case Report of Takayasu Arteritis Manifesting as a Vascular Enigma

Vanessa Pasadyn, BA, Samantha Davis, MD, Rawish Fatima, MD, Nezam Altorok, MD
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Abstract

Introduction Takayasu arteritis (TKA) is a rare large vessel vasculitis, most prevalent in Asia and affecting females ages 10-40 years. Through unclear etiology, it triggers chronic granulomatous inflammation leading to vessel wall thickening, stenosis, and occlusion. Manifestations vary from mild malaise to severe ischemic complications. Diagnosis hinges on clinical criteria, including angiography, and exclusion of mimicking conditions like giant cell arteritis, fibromuscular dysplasia, or atherosclerosis. Treatment necessitates immunosuppression and anti-inflammatories to curb disease progression and limit complications. Case Presentation A 61-year-old Caucasian female presented with claudication of the upper extremities upon using the shower. She reported episodes of headache, myalgia, fever and chills of several months. She reported fatigue with overhead reaching and difficulty finding her pulse on her upper extremities. Labs were notable for elevated ESR and CRP. MRA chest showed smoky thickened appearance of the descending aorta wall, some missing wall thickening in origins of the left common carotid and left subclavian arteries. PET scan revealed diffuse hypermetabolic activity involving the bilateral common carotid arteries, peripheral aortic arch and descending thoracic aorta (Figure 1). With these ongoing symptoms and characteristic features on imaging, we established the diagnosis of TKA. She was started on 5mg oral prednisone daily and methotrexate 10mg weekly with daily folic acid. Conclusion This case highlights the diagnosis and treatment of a rare condition, Takayasu arteritis, the pulseless disease. TKA is a challenging condition to study and understand fully, but advancements in medical knowledge, imaging, and management are gradually improving our understanding and ability to diagnose and treat this condition. With increased awareness of this condition, earlier detection and monitoring will serve to benefit future patient populations.
揭开 "沉默的收缩器 "的神秘面纱:表现为血管之谜的高安动脉炎病例报告
导言 高安动脉炎(TKA)是一种罕见的大血管炎,多发于亚洲,好发于 10-40 岁的女性。由于病因不明,它会引发慢性肉芽肿性炎症,导致血管壁增厚、狭窄和闭塞。表现从轻微不适到严重缺血并发症不等。诊断取决于临床标准,包括血管造影,并排除巨细胞动脉炎、纤维肌发育不良或动脉粥样硬化等模仿性疾病。治疗时必须使用免疫抑制剂和抗炎药物,以遏制病情发展和减少并发症。病例介绍 一位 61 岁的白种女性因淋浴时上肢跛行而就诊。她报告说头痛、肌痛、发烧和发冷已持续数月。她报告说,上肢伸展时感到疲劳,而且难以找到脉搏。实验室检查显示血沉和 CRP 升高。胸部 MRA 显示降主动脉壁呈烟雾状增厚,左侧颈总动脉和左侧锁骨下动脉起源处有一些缺失的壁增厚。正电子发射计算机断层扫描显示,双侧颈总动脉、外周主动脉弓和降主动脉存在弥漫性高代谢活动(图 1)。根据这些持续存在的症状和影像学特征,我们确定了 TKA 的诊断。她开始每天口服 5 毫克泼尼松,每周口服 10 毫克甲氨蝶呤,每天服用叶酸。结论 本病例强调了一种罕见疾病--高安动脉炎(无脉疾病)的诊断和治疗。TKA 是一种难以全面研究和理解的疾病,但医学知识、影像学和管理方面的进步正在逐步提高我们对这种疾病的理解和诊断治疗能力。随着人们对这种疾病认识的提高,更早地发现和监测这种疾病将造福于未来的患者群体。
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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