Pediatr Infect Vaccine.  2022 Dec;29(3):166-172. 10.14776/piv.2022.29.e22.

A Boy With Blau Syndrome Misdiagnosed as Refractory Kawasaki Disease

Affiliations
  • 1Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, the Republic of Korea
  • 2Department of Pediatrics, Korea University Guro Hospital, College of Medicine, Korea University, Seoul, the Republic of Korea
  • 3Department of Pediatrics, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin, the Republic of Korea
  • 4Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, the Republic of Korea
  • 5Department of Child Health and Development, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan

Abstract

Blau syndrome is a systemic autoinflammatory disease presenting with non-caseating granulomatous dermatitis, chronic uveitis, and arthritis. It is caused by a gain-of-function variant of the nucleotide-binding oligomerization domain protein 2 gene, which leads to the overactivation of inflammatory cytokines and eventually causes autoinflammation. Since the symptoms of Blau syndrome are nonspecific and usually do not appear simultaneously, it is challenging to differentiate Blau syndrome from other inflammatory disorders. This is a case report of a 13-month-old boy who had suffered from recurrent skin rash and fever. The patient was previously misdiagnosed as refractory Kawasaki disease twice and was treated with intravenous immunoglobulin and systemic glucocorticoid, which only resulted in transient improvement of the symptoms. He was eventually diagnosed with Blau syndrome.

Keyword

Skin rash; Uveitis; Arthritis; Sarcoidosis; Kawasaki disease
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