Jacob J L, Polomeno R C, Chad Z, Lapointe N
Can J Ophthalmol. 1982 Oct;17(5):199-202.
This paper describes nine patients, five girls and four boys aged 4 months to 7 years (mean 3 3/4 years), who had the clinical and laboratory features of Kawasaki disease (mucocutaneous lymph node syndrome). Eight of them had mild to moderate anterior uveitis, and one child showed choroidal, retinal and vitreous changes in one eye that caused a severe visual loss. Recognition of this disease is important, particularly since 1% to 2% of patients under 2 years of age die suddenly from coronary arteritis.
本文描述了9名患者,5名女孩和4名男孩,年龄在4个月至7岁之间(平均3又3/4岁),他们具有川崎病(黏膜皮肤淋巴结综合征)的临床和实验室特征。其中8人患有轻度至中度前葡萄膜炎,1名儿童一只眼睛出现脉络膜、视网膜和玻璃体改变,导致严重视力丧失。认识这种疾病很重要,特别是因为2岁以下的患者中有1%至2%会突然死于冠状动脉炎。