An adolescent case of Kawasaki disease after Japanese en­ceph­a­li­tis vaccination

Madoka Shirai, Aiko Honda, Toshiyuki Takagi, Megumi Okawa, Yuki Okada
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Abstract

Kawasaki disease (KD) is a systemic vasculitis syndrome that predominantly affects infants. In Japan, more than 10,000 people are diagnosed with KD annually, and the number is increasing. However, its etiology remains unidentified. In this report, we describe a KD case that developed after Japanese encephalitis vaccination in an adolescent boy. The patient was a generally healthy 14-year-old boy who experienced fever and erythematous extremities 11h after Japanese encephalitis vaccination. Initially, his symptoms were followed up as an adverse reaction to the vaccination. However, his symptoms did not improve, and on day 4 of the fever, he exhibited five of six major symptoms of KD. After intravenous administration of immunoglobulin and acetylsalicylic acid, his symptoms gradually resolved. Although KD development after vaccination in adolescents is rare, it should be considered a differential diagnosis.
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日本接种乙脑疫苗后发生川崎病1例
川崎病(KD)是一种主要影响婴儿的系统性血管炎综合征。在日本,每年有超过1万人被诊断患有KD,而且这个数字还在增加。然而,其病因尚不清楚。在本报告中,我们描述了一例在接种日本脑炎疫苗后发生的KD病例。患者是一名健康的14岁男孩,在接种日本脑炎疫苗11小时后出现发热和四肢红斑。最初,他的症状作为接种疫苗的不良反应被跟踪。然而,他的症状没有改善,在发烧的第4天,他出现了KD的6个主要症状中的5个。经静脉注射免疫球蛋白及乙酰水杨酸后,症状逐渐消失。虽然青少年接种疫苗后发生KD很少见,但它应被视为一种鉴别诊断。
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