Abstract
Chronic granulomatous disease (CGD) is an infrequent inherited disorder characterized by recurrent infections and abnormal granuloma formation. Patients with CGD have an exuberant inflammatory response and an increased risk of developing autoimmunity. We present the case of a 1-year-old boy with CGD who developed several of the characteristic clinical features of Kawasaki Disease. His illness responded to intravenous immunoglobulin, aspirin, and corticosteroids.
MeSH Terms
Comorbidity
Drug Therapy, Combination
Glucocorticoids/therapeutic use
Granulomatous Disease, Chronic/drug therapy,epidemiology
Humans
Immunoglobulins, Intravenous/therapeutic use
Immunologic Factors/therapeutic use
Infant
Male
Mucocutaneous Lymph Node Syndrome/drug therapy,epidemiology,etiology
Prednisolone/therapeutic use
Chemicals
Glucocorticoids
Immunoglobulins, Intravenous
Immunologic Factors
Prednisolone
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Yamazaki-Nakashimada M A
Department of Clinical Immunology, Instituto Nacional de Pediatría, Insurgentes Sur 3700-C C.P, 04530, Col. Insurgentes Cuicuilco, Mexico City, Mexico. yzki71@yahoo.com.mx
Ramírez-Vargas N
De Rubens-Figueroa J
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