川崎病(KD)又称皮肤黏膜淋巴结综合征,是小儿时期较为常见的自身免疫性疾病,病理特征为全身广泛的中小血管免疫性炎症,可致多系统损害,尤以心脏冠状动脉(冠脉)受累最为常见,已成为小儿后天性心脏病的常见原因之一[1-2]。虽然KD引起的冠脉损害广受关注,但合并心功能不全的报道很少见。广东省中山市博爱医院儿科近10年收治KD476例,合并心功能不全3例。现报道如下。 Kawasaki disease (KD), also known as mucocutaneous lymph node syndrome, is a more common autoimmune disease in infancy and is characterized by a wide range of systemic autoimmune inflammation of the small and medium-sized vessels that can cause multiple system damage, especially in the coronary arteries ) The most common involvement has become a common cause of acquired heart disease in children [1-2]. Although KD-induced coronary artery lesions have drawn much attention, reports of cardiac insufficiency have been rare. Pok Oi Hospital, Zhongshan City, Guangdong Province pediatric nearly 10 years admitted KD476 cases, 3 cases of cardiac insufficiency. Report as follows now.