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CASE REPORT article

Front. Pediatr.

Sec. General Pediatrics and Pediatric Emergency Care

Volume 13 - 2025 | doi: 10.3389/fped.2025.1652101

Development of mild encephalitis with a reversible splenial lesion prior to the diagnosis of Kawasaki disease: A pediatric case report

Provisionally accepted
Hirokazu  YamanouchiHirokazu Yamanouchi1Sagano  OnoyamaSagano Onoyama2*Kentaro  MarutaniKentaro Marutani3Nobutaka  HaradaNobutaka Harada2Hikaru  KanemasaHikaru Kanemasa2Yuji  UenoYuji Ueno3Ryutaro  KiraRyutaro Kira3Shuya  KanekoShuya Kaneko4Masaki  ShimizuMasaki Shimizu5Takayuki  HoshinaTakayuki Hoshina6
  • 1Kawasaki Disease Center, Fukuoka Children’s Hospital, Fukuoka, Japan
  • 2Pediatric Infectious Diseases and Immunology, Fukuoka Children’s Hospital, Fukuoka, Japan
  • 3Pediatric Neurology, Fukuoka Children’s Hospital, Fukuoka, Japan
  • 4Pediatric and Development Biology, Tokyo Kagaku Daigaku Byoin, Bunkyo, Japan
  • 5Department of Pediatrics, Perinatal and Maternal Medicine, Tokyo Kagaku Daigaku Byoin, Bunkyo, Japan
  • 6General Medial Department, Fukuoka Children’s Hospital, Fukuoka, Japan

The final, formatted version of the article will be published soon.

Kawasaki disease (KD) rarely causes neurological complications. KD is diagnosed based on symptoms alone and can be very difficult to diagnose if other symptoms appear in febrile children before the main symptoms of KD. A 5-year-old boy with fever and consciousness disturbance was hospitalized and diagnosed with mild encephalitis/encephalopathy with reversible splenial lesion (MERS). The fever and consciousness disturbance resolved with intravenous methylprednisolone for 3 days (30 mg/kg/day) and intravenous immunoglobulin (IVIG; 1 g/kg/day) for 2 days, which was initiated as treatment for MERS. However, bilateral conjunctival injections, redness of the lips, and membranous desquamation of the fingers were observed, followed by recurrence of fever four days after the initial treatment. Echocardiography revealed dilation of the right coronary artery (RCA). The patient was diagnosed with incomplete KD and was treated with high-dose IVIG and oral aspirin based on the presence of four major KD symptoms and coronary artery dilation. After treatment, he showed defervescence, and the RCA showed no further dilation on echocardiography. Clinicians should recognize that the development of MERS may precede the diagnosis of KD in some patients. In addition, patients with MERS of unknown etiology, leukocytosis, and elevated serum CRP levels should be closely monitored because of the possibility of KD.

Keywords: kawasaki disease, mild encephalitis with a reversible splenial lesion, Coronary artery abnormality, Intravenous Immunoglobulin, case report, Presenting symptoms

Received: 23 Jun 2025; Accepted: 28 Jul 2025.

Copyright: © 2025 Yamanouchi, Onoyama, Marutani, Harada, Kanemasa, Ueno, Kira, Kaneko, Shimizu and Hoshina. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Sagano Onoyama, Pediatric Infectious Diseases and Immunology, Fukuoka Children’s Hospital, Fukuoka, Japan

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