Tseng C F, Fu Y C, Fu L S, Betau H, Chi C S
Department of Pediatrics, Taichung Veterans General Hospital, 160, Sec. 3, Taichung-Kang Road, Taichung 407, Taiwan.
Zhonghua Yi Xue Za Zhi (Taipei). 2001 Mar;64(3):168-73.
Kawasaki disease is a common acquired heart disease in children. Only a few reports have been published concerning Kawasaki disease in infants. This study was performed to assess the clinical spectrum of Kawasaki disease in infants.
Between January 1989 and December 1998, a total of 48 consecutive Kawasaki patients less than one year of age were enrolled and studied retrospectively. Coronary artery dilation was defined as the internal diameter of a coronary artery larger than 3 mm. All cases received 2 gm/Kg of intravenous immunoglobulin. We divided the patients into two groups; group I; coronary artery dilation (+) and group II; coronary artery dilation (-), and compared the clinical and laboratory data.
Of 273 patients with Kawasaki disease, 48 (17.5%) were less than one year of age. Among these patients (< 1 year old), the median age was 7.8 +/- 2.8 months (range 2 months to 12 months), and the male to female ratio was 1.52:1. The incidence of atypical Kawasaki disease was 31.2% (compared with an incidence of atypical Kawasaki disease among patient more than one year of age of 7.5%; p < 0.001), and that of coronary artery dilation was 35.4%. Clinical manifestations included fever 100%, extremity change 91.6%, skin rash 89.6%, conjunctivitis 89.6%, oral mucosa change 89.6%, and cervical lymphadenopathy 0%. Laboratory data revealed white blood cell count: 15,403 +/- 6,282/mm3, hemoglobin: 10.1 +/- 1.0 gm/dl, neutrophil: 59.2 +/- 13.7%, lymphocytes: 30.6 +/- 13.1%, platelet count: 456,3000 +/- 216,4000/mm3, and C-reactive protein 8.2 +/- 5.6 mg/dl. Patients with coronary artery dilation had a longer duration of diagnosis, higher incidence of atypical presentation, lower incidence of conjunctivitis, lower incidence of skin rash, lower incidence of extremity change, and lower C-reactive protein. The predictive value of coronary artery dilation based on the combination of atypical presentation, duration of diagnosis, and C-reactive protein was 81.2%.
Kawasaki disease in infants is associated with a high incidence of atypical presentation and increased risk of coronary artery dilation. We suggest that in an infant with insufficient diagnostic criteria for Kawasaki disease, care should be taken to avoid missing atypical Kawasaki disease. Echocardiography is an important tool for diagnosis of atypical Kawasaki disease.
川崎病是儿童常见的后天性心脏病。关于婴儿川崎病的报道较少。本研究旨在评估婴儿川崎病的临床特征。
1989年1月至1998年12月,共纳入48例年龄小于1岁的川崎病患儿并进行回顾性研究。冠状动脉扩张定义为冠状动脉内径大于3mm。所有病例均接受2g/kg静脉注射免疫球蛋白治疗。我们将患者分为两组;I组:冠状动脉扩张(+)组和II组:冠状动脉扩张(-)组,并比较临床和实验室数据。
在273例川崎病患者中,48例(17.5%)年龄小于1岁。在这些小于1岁的患者中,中位年龄为7.8±2.8个月(范围2个月至12个月),男女比例为1.52:1。非典型川崎病的发生率为31.2%(1岁以上患者中非典型川崎病的发生率为7.5%;p<0.001),冠状动脉扩张的发生率为35.4%。临床表现包括发热100%、四肢变化91.6%、皮疹89.6%、结膜炎89.6%、口腔黏膜变化89.6%、颈部淋巴结肿大0%。实验室数据显示白细胞计数:15403±6282/mm³、血红蛋白:10.1±1.0g/dl、中性粒细胞:59.2±13.7%、淋巴细胞:30.6±13.1%、血小板计数:4563000±2164000/mm³、C反应蛋白8.2±(此处原文可能有误,推测应为5.6)mg/dl。冠状动脉扩张的患者诊断持续时间更长、非典型表现发生率更高、结膜炎发生率更低、皮疹发生率更低、四肢变化发生率更低、C反应蛋白更低。基于非典型表现、诊断持续时间和C反应蛋白联合判断冠状动脉扩张的预测价值为81.2%。
婴儿川崎病与非典型表现的高发生率及冠状动脉扩张风险增加相关。我们建议,对于诊断标准不充分的婴儿川崎病患者,应注意避免漏诊非典型川崎病。超声心动图是诊断非典型川崎病的重要工具。