Kawasaki Disease Following Severe Sunburn Injury
Author(s) -
Seigo Okada,
Shintaro Hashimoto,
Akiko Miyake,
Yusuke Okada,
Reiji Hirano,
Shinnosuke Fukunaga,
Yuichi Ishikawa
Publication year - 2020
Publication title -
frontiers in pediatrics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.96
H-Index - 36
ISSN - 2296-2360
DOI - 10.3389/fped.2020.00006
Subject(s) - medicine , etiology , innate immune system , sunburn , disease , kawasaki disease , immunology , vasculitis , immune dysregulation , immunity , immune system , dermatology , artery
Background: Although an etiology of Kawasaki disease (KD) is unknown, an aberrant innate immune system in predisposed individuals has been proposed to play a key role in the development of KD vasculitis. Various etiological pathogens have been proposed as the trigger of KD and a scaled injury preceding symptom onset has been reported as one of them. Here, we report a 17-month-old Japanese female who was hospitalized due to high fever lasting for 4 days with infection ruled out as a cause. On admission, she displayed severe sunburn all over her body following a prolonged period of outdoor play 5 days ago. On the 5 day of illness, she developed complete KD. Serum levels of high mobility group box 1, a representative for damage-associated molecular patterns (DAMPs), were elevated during acute phase and continued to decrease during subacute phase. This unique course suggested the inflammatory process of KD involving innate immunity via DAMPs.
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