Mărginean Cristina O, Meliț Lorena E, Gozar Liliana, Mărginean Cristian Dan, Mărginean Maria O
Department of Pediatrics, University of Medicine and Pharmacy TîrguMures, Târgu Mures, Romania.
Department of Pediatric Cardiology, University of Medicine and Pharmacy TîrguMures, Târgu Mures, Romania.
Front Pediatr. 2018 Jul 27;6:210. doi: 10.3389/fped.2018.00210. eCollection 2018.
Kawasaki disease (KD) is a febrile vasculitis, which is commonly defined by fever and at least four specific clinical symptoms. Incomplete KD is defined by suggestive echocardiographic findings with an incomplete clinical picture. Refractory KD is diagnosed in patients resistant to intravenous immunoglobulin (IVIG). We report the case of a 6-month-old male infant admitted to our clinic for persistent fever and onset of a generalized polymorphous rash, accompanied by high fever, rhinorrhea, and cough for the past 7 days. The laboratory tests, on the day of admission, revealed leukocytosis with neutrophilia, anemia, thrombocytosis, hypernatremia, hypoalbuminemia, elevated C-reactive protein (CRP), and erythrocyte sedimentation rate (ESR). Echocardiography showed dilation of the left anterior descending coronary artery (LAD). Based on all these findings, we established the diagnosis of KD, and we initiated IVIG and intravenous pulsed methylprednisolone, with an initial favorable outcome. However, the symptoms reappeared, and we administered a second higher single dose of IVIG, but without any clinical improvement. Moreover, the laboratory parameters and echocardiographic findings worsened. We reinitiated a longer course of intravenous methylprednisolone in a smaller dose, which had a favorable impact on the clinical, laboratory, and echocardiographic parameters. Multiple uncertainties exist related to the management of refractory KD despite the wide spectrum of therapeutic options that have been proposed. Our case demonstrates that in patients refractory to aggressive initial therapy, low or moderate doses of steroid given daily may be helpful.
川崎病(KD)是一种发热性血管炎,通常由发热和至少四种特定临床症状定义。不完全KD由具有不完全临床表现的提示性超声心动图结果定义。难治性KD在对静脉注射免疫球蛋白(IVIG)耐药的患者中诊断。我们报告一例6个月大男婴,因持续发热和全身性多形性皮疹入院,过去7天伴有高热、流涕和咳嗽。入院当天的实验室检查显示白细胞增多伴中性粒细胞增多、贫血、血小板增多、高钠血症、低白蛋白血症、C反应蛋白(CRP)升高和红细胞沉降率(ESR)升高。超声心动图显示左前降支冠状动脉(LAD)扩张。基于所有这些发现,我们确诊为KD,并开始使用IVIG和静脉注射脉冲甲基强的松龙,初始效果良好。然而,症状再次出现,我们给予了更高剂量的单次IVIG,但临床无改善。此外,实验室参数和超声心动图结果恶化。我们重新开始使用较小剂量的较长疗程静脉注射甲基强的松龙,这对临床、实验室和超声心动图参数产生了有利影响。尽管已提出了广泛的治疗选择,但难治性KD的管理仍存在多个不确定性。我们的病例表明,对于初始积极治疗无效的患者,每日给予低剂量或中等剂量的类固醇可能会有帮助。