Coronary artery bypass grafting in a child with Kawasaki disease

Pedro Magro , Nuno Carvalho , Rui Anjos , José Neves
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Abstract

Kawasaki disease (KD) with cardiac involvement can result in the development of coronary aneurysm, stenosis or thrombosis with significant cardiovascular implications. We report the case of a 23-month-old male with a late diagnosis of KD, in whom intravenous immunoglobulin treatment was not feasible. The patient's course was assessed by routine echocardiography. At the age of five years, angiographic assessment revealed an aneurysm of the anterior descending coronary artery measuring 17 mm×7 mm involving the first diagonal branch, 90% post-aneurysmal stenosis, and an aneurysm of the right coronary artery measuring 32 mm×6 mm. Due to the critical anatomy of the anterior descending artery the revascularization method of choice was coronary artery bypass surgery with an internal mammary artery graft, under cardiopulmonary bypass. There were no significant intraoperative or postoperative complications. This confirms coronary artery bypass grafting as a reliable treatment option for patients who present with coronary sequelae from KD, even at a very young age.

川崎病患儿冠状动脉旁路移植术1例
川崎病累及心脏可导致冠状动脉瘤、狭窄或血栓形成,具有明显的心血管影响。我们报告一例23个月大的男性与晚期诊断的KD,在静脉免疫球蛋白治疗是不可行的。通过常规超声心动图评估患者的病程。5岁时,血管造影显示冠状动脉前降支动脉瘤直径17 mm×7 mm,累及第一斜支,90%动脉瘤后狭窄,右冠状动脉动脉瘤直径32 mm×6 mm。由于前降支的关键解剖结构,首选的血运重建方法是在体外循环下进行冠状动脉搭桥手术并植入乳腺内动脉。术中、术后均无明显并发症。这证实了冠状动脉旁路移植术对于患有KD的冠状动脉后遗症的患者是一种可靠的治疗选择,即使是在非常年轻的年龄。
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