A 14.5-Year-Old Boy with Coronary Obstruction after Kawasaki Disease: A Case Report.

Mohammad Reza Sabri, Chehreh Mahdavi, Alireza Ahmadi, Mehdi Ghaderian, Bahar Dehghan
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Abstract

Kawasaki disease (KD) is a febrile vasculitis and is considered a leading cause of acquired coronary artery disease in children. A clinically critical complication is the coronary artery aneurysm, which may progress and lead to coronary stenosis or even obstruction. Herein, we describe a 14.5-year-old boy with a history of KD at 6 months old, who developed multiple aneurysms along all the coronary branches. During the follow-up at the age of 14 years, the left coronary artery aneurysms regressed, while the aneurysm of the right coronary artery persisted and was complicated by obstruction at its proximal part, according to computed tomography angiography. However, the patient at the last follow-up was asymptomatic and well. The serious nature of KD coronary complications warrants follow-up visits. Since echocardiography alone may fail to reveal stenosis or obstruction, other adjunct follow-up imaging modalities such as conventional, computed tomography, and magnetic resonance angiography should be performed in patients with coronary aneurysms.

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14.5岁男童川崎病后冠状动脉阻塞1例。
川崎病(KD)是一种发热性血管炎,被认为是儿童获得性冠状动脉疾病的主要原因。临床上重要的并发症是冠状动脉动脉瘤,它可能发展并导致冠状动脉狭窄甚至梗阻。在此,我们描述了一个14.5岁的男孩,在6个月大时有KD病史,他在所有冠状动脉分支上出现了多个动脉瘤。在14岁的随访中,左侧冠状动脉动脉瘤消退,而右侧冠状动脉动脉瘤持续存在,并合并近端梗阻。然而,患者在最后一次随访时无症状且状况良好。KD冠状动脉并发症的严重性值得随访。由于超声心动图本身可能无法显示狭窄或梗阻,其他辅助随访成像方式,如常规、计算机断层扫描和磁共振血管造影,应在冠状动脉瘤患者中进行。
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
Journal of Tehran University Heart Center
Journal of Tehran University Heart Center Medicine-Cardiology and Cardiovascular Medicine
CiteScore
0.90
自引率
0.00%
发文量
46
审稿时长
12 weeks
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