Kawasaki disease and immunodeficiencies in children: case reports and literature review.
Francisco Eduardo Rivas-LarrauriJacqueline Lorena Aguilar-ZanelaPaola Castro-OteoLuis Adrian Rosales-HernandezFrancisco Otero-MendozaGabriela López-HerreraJavier Ordoñez-OrtegaLuis Martín Garrido-GarcíaMarco Antonio Yamazaki-NakashimadaPublished in: Rheumatology international (2019)
Kawasaki disease (KD) has features that appear supporting an infectious cause with a secondary deranged inflammatory/autoimmune response. The association of KD in adults with human immunodeficiency virus infection and the presence of KD in patients with immunodeficiency disorders support the infectious theory. We present four KD patients associated with immunodeficiencies: one with X-linked agammaglobulinemia, one with HIV infection, and two with leukemia; one of these patients also had Down syndrome. We did a literature search to find out all reported cases of immunodeficiency with KD in children. In immunodeficiency disorders, the inability of the immune system to eradicate the pathogens coupled to an exaggerated inflammatory response, especially in chronic granulomatous disease, may lead to the development of KD. The study of patients with immunodeficiencies complicated with KD may shed light into the etiopathogenesis of the disease.
Keyphrases
- end stage renal disease
- inflammatory response
- ejection fraction
- newly diagnosed
- chronic kidney disease
- endothelial cells
- prognostic factors
- young adults
- case report
- peritoneal dialysis
- rheumatoid arthritis
- multiple sclerosis
- lipopolysaccharide induced
- systemic sclerosis
- patient reported
- antimicrobial resistance
- multidrug resistant
- lps induced