Petrarca L, Nenna R, Versacci P, Frassanito A, Cangiano G, Nicolai A, Scalercio F, Russo L Lo, Papoff P, Moretti C, Midulla F
Department of Pediatrics, "Sapienza" University of Rome, V.le Regina Elena 324, 00161, Rome, Italy.
Ital J Pediatr. 2017 Mar 8;43(1):30. doi: 10.1186/s13052-017-0345-0.
Kawasaki disease (KD) is an acute inflammatory vasculitis of unknown origin.
We report the case of a 5-month-old child with an atypical form of KD, characterized by undulating symptoms, who developed an aneurysm of the right coronary artery and an ectasia of the left anterior descending coronary artery.
This case report underlines the difficulties in recognizing incomplete forms of the illness in young infants, who are at higher risk of cardiac complications.
川崎病(KD)是一种病因不明的急性炎症性血管炎。
我们报告一例5个月大非典型川崎病患儿,其症状呈波动状,并发右冠状动脉瘤及左前降支冠状动脉扩张。
本病例报告强调了识别婴幼儿不完全型川崎病的困难,这类患儿发生心脏并发症的风险更高。