| Tóm tắt: | Naser Gharebaghi,1 Miramir Aghdashi,2 Seyed Arman Seyed Mokhtari3 1Department of Infectious Disease, Faculty of Medicine, Urmia University of Medical Science, Urmia, Iran; 2Department of Rheumatology and Internal Medicine, Faculty of Medicine, Urmia University of Medical Science, Urmia, Iran; 3Student Research Committee, Urmia University of Medical Sciences, Urmia, Iran Abstract: Kawasaki disease (KD) is characterized with an acute systemic vasculitis of the medium- and small-sized vessels. This disease mainly involves children within the age of 6 months to 5 years and it is often self-limited and patients seem to recover well; however, it may lead to devastating and fatal cardiovascular complications such as coronary artery aneurysm. Thus, early diagnosis and appropriate management of this disease have a significant effect on improving the prognosis and preventing its serious complications. Adult-onset KD (AKD) is rare and often misdiagnosed. Here we report a rare case of KD that occurred in a 17-year-old young adult who presented 4 weeks post splenectomy, with clinical signs and symptoms consistent with AKD. This may potentially highlight the association of AKD with infectious etiologies. Keywords: Kawasaki disease, adult, splenectomy
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