Abstract
Kawasaki disease is an acute vasculitis of childhood. Macrophage activation syndrome is a rare life threatening complication. In this article, we report a five-year-six-month old girl patient with Kawasaki disease who developed irritability, hepatosplenomegaly, and pancytopenia after treatment with intravenous immunoglobulins. Patient’s blood test and bone marrow aspiration results suggested macrophage activation syndrome. The patient responded to dexamethasone in a dose of 10 mg/m2/day.
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Article Info
Published In
Journal
Archives of Rheumatology
Volume / Issue
Volume 30 · Issue 2 · June 2015
Pages
178-180
History
Published Online
June 30, 2015
License

This work is licensed under a Creative Commons Attribution 4.0 International License.
Affiliations
1
Kallol BOSE
Department of Pediatrics, Chittaranjan Seva Sadan Hospital, West Bengal, India
2
Sudip SAHA
Department of Pediatrics, Chittaranjan Seva Sadan Hospital, West Bengal, India
3
Prabir SAHA
Department of Pediatrics, Chittaranjan Seva Sadan Hospital, West Bengal, India
4
Piyasi MONDAL
Department of Pediatrics, Chittaranjan Seva Sadan Hospital, West Bengal, India
Cite this Article
Kallol BOSE, Sudip SAHA, Prabir SAHA, & Piyasi MONDAL. (2015). Macrophage Activation Syndrome: A Potentially Fatal Complication of Kawasaki Disease. Archives of Rheumatology, 30(2), 178–180. https://doi.org/10.5606/ArchRheumatol.2015.5186
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