Abstract
Immunoglobulin IgA vasculitis, also known as Henoch-Schönlein purpura, is the most prevalent type of systemic vasculitis in children and typically develops between the ages of 3 and 15. The reports of its occurrence in adults is rare. The low prevalence in adults is probably due to misdiagnosis or improper diagnosis. In order to properly manage patients and prevent its related complications, physicians should be able to correctly identify IgA vasculitis in addition to the pediatricians. There is still some research to be done on the management of adult-onset IgA vasculitis with multi organ involvement. Here, we report a case series of three adult-onset IgA vasculitis cases that were triggered by different elements
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