Lörincz G, Hill K, Schaper G
Dtsch Med Wochenschr. 1979 Oct 26;104(43):1518-20. doi: 10.1055/s-0028-1129134.
In a 2-year 4-month-old boy endarteritic changes and spindle-shaped aneurysmas of the coronary arteries were found as a complication of Kawasaki syndrome. The vascular alteration, probably immunopathologically based, must be differentiated as a primary endarteritic process from primary necrotising periateritis nodosa which also occurs in childhood. The fate of the affected children is determined by the complications of coronary artery changes which however occur only in 1--2% of affected persons.
在一名2岁4个月大的男孩中,发现冠状动脉内膜炎改变和梭形动脉瘤是川崎综合征的并发症。这种血管改变可能基于免疫病理学,必须与儿童期也会出现的原发性结节性动脉周围炎这种原发性动脉内膜炎过程相鉴别。患病儿童的预后取决于冠状动脉改变的并发症,然而这些并发症仅发生在1% - 2%的患病个体中。