Recurrent Stroke as a Presenting Feature of Takayasu Arteritis in an Adolescent: A Case Report and Literature Review.

Q4 Biochemistry, Genetics and Molecular Biology
Vasiliki Sgouropoulou, Efthymia Vargiami, Maria Kyriazi, Sofia Kafterani, Stella Stabouli, Georgios Tsigaras, Athanasia Anastasiou, Maria Trachana, Dimitrios Zafeiriou
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引用次数: 0

Abstract

Takayasu arteritis is a large vessel vasculitis, characterized by granulomatous inflammation of arterial vessels, that typically affects the aorta, its main branches and pulmonary arteries. Disease diagnosis is a challenge and requires awareness of the condition, as clinical signs can be not specific. We report a case of an adolescent with recurrent stroke diagnosed with Takayasu arteritis. A diagnosis of Takayasu arteritis was established due to angiographic findings in the magnetic resonance angiography in conjunction with systolic blood pressure discrepancy, arterial hypertension and increased acute phase reactants. Takayasu arteritis is a rare cause of ischemic stroke in children. However, stroke may be the first manifestation of the disease. Clinical experience and multidisciplinary approach, including aggressive treatment, is essential for the favourable outcome of the disease and the reduction of the associated morbidity and mortality.

作为青少年高安动脉炎表现特征的复发性中风:病例报告与文献综述
高安动脉炎是一种大血管炎,以动脉血管肉芽肿性炎症为特征,通常累及主动脉及其主要分支和肺动脉。疾病诊断是一项挑战,需要对病情有所了解,因为临床表现可能不具特异性。我们报告了一例青少年反复中风患者被诊断为高安动脉炎的病例。由于磁共振血管造影的血管造影结果与收缩压差异、动脉高血压和急性期反应物增高相结合,确定了高安动脉炎的诊断。高安动脉炎是儿童缺血性中风的罕见病因。然而,中风可能是该病的首发表现。临床经验和多学科方法,包括积极治疗,对于疾病的良好预后以及降低相关发病率和死亡率至关重要。
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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来源期刊
Prague medical report
Prague medical report Medicine-Medicine (all)
CiteScore
1.10
自引率
0.00%
发文量
19
审稿时长
20 weeks
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