Evidence map›Paper›PMID 40881803›Full record

ArticleFrontiers in pediatrics2025

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

Hirokazu Yamanouchi, Sagano Onoyama, Kentaro Marutani, Nobutaka Harada, Yuji Ueno, Hikaru Kanemasa, Ryutaro Kira, Shuya Kaneko, Masaki Shimizu, Takayuki Hoshina

Abstract readCase Reports
In one paragraph

Article in Frontiers in pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Hirokazu YamanouchiKawasaki Disease Center, Fukuoka Children's Hospital, Fukuoka, Japan.
Sagano OnoyamaKawasaki Disease Center, Fukuoka Children's Hospital, Fukuoka, Japan.
Kentaro MarutaniDepartment of Pediatric Neurology, Fukuoka Children's Hospital, Fukuoka, Japan.
Nobutaka HaradaKawasaki Disease Center, Fukuoka Children's Hospital, Fukuoka, Japan.
Yuji UenoDepartment of Pediatric Neurology, Fukuoka Children's Hospital, Fukuoka, Japan.
Hikaru KanemasaKawasaki Disease Center, Fukuoka Children's Hospital, Fukuoka, Japan.
Ryutaro KiraDepartment of Pediatric Neurology, Fukuoka Children's Hospital, Fukuoka, Japan.
Shuya KanekoDepartment of Pediatrics and Developmental Biology, Institute of Science Tokyo, Tokyo, Japan.
Masaki ShimizuDepartment of Pediatrics, Perinatal and Maternal Medicine, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, Japan.
Takayuki HoshinaKawasaki Disease Center, Fukuoka Children's Hospital, Fukuoka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

case reportcoronary artery abnormalityintravenous immunoglobulinKawasaki diseasemild encephalitis with a reversible splenial lesionpresenting symptoms

Identifiers

PMID40881803
PMCPMC12380580

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