Abstract
Intravenous immunoglobulin (IVIG) is a standard therapy for Kawasaki disease (KD), because it prevents formation of coronary artery aneurysm, a major complication of KD. Herein, we report a 3-year-old boy with KD complicated by haemolytic anaemia (HA) which developed following two courses of IVIG. Although both direct and indirect antiglobulin tests and anti-M antibodies were positive in his blood obtained after the onset of HA, indirect antiglobulin tests and anti-M antibodies were negative either in the blood sample before the treatment or the same lot of IVIG products as those used for the therapy, suggesting autoimmune mechanism. This is, to our knowledge, the first report of autoimmune HA caused by anti-M autoantibodies after IVIG therapy in KD.
Acknowledgements
The authors thank Dr. H. Azuma, Asahikawa Medical University, for his insightful comments.
Patient consent
A written informed consent for publication of this report was obtained from the patient’s parents.
Ethical approval
Not Applicable.
Conflict of interest
None.
Correction Statement
This article has been republished with minor changes. These changes do not impact the academic content of the article.