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J Pediatr Hematol Oncol ; 43(3): e448-e451, 2021 04 01.
Article in English | MEDLINE | ID: mdl-32079989

ABSTRACT

Kawasaki disease (KD) is an acute systemic vasculitis of unknown etiology. KD can be complicated with macrophage activation syndrome. The optimal treatment for this KD complication has not been established, and a variety of treatments have been used. Infliximab, a chimeric monoclonal antibody that binds tumor necrosis factor, has proved to be efficacious in IV gammaglobulin resistant KD. We present 2 cases of KD complicated with macrophage activation syndrome, including 1 patient with DiGeorge syndrome successfully treated with a combined treatment of IV gammaglobulin, corticosteroids, cyclosporine, and infliximab.


Subject(s)
Dermatologic Agents/therapeutic use , Infliximab/therapeutic use , Macrophage Activation Syndrome/drug therapy , Mucocutaneous Lymph Node Syndrome/drug therapy , Adrenal Cortex Hormones/therapeutic use , Adult , Child, Preschool , Cyclosporine/therapeutic use , Female , Humans , Immunoglobulins, Intravenous/therapeutic use , Macrophage Activation Syndrome/complications , Male , Mucocutaneous Lymph Node Syndrome/complications , Young Adult
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