Henoch-Schonlein purpura (HSP) is the most common systemic vasculitis in childhood. There is no consensus about the management for isolated cutaneous manifestations in HSP. We describe a case of HSP presenting with severe skin lesions that did not respond to standard therapy with corticosteroids. The 11-year-old child was treated with intravenous immunoglobulins, which induced rapid and persistent resolution of symptomatology.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1111/pde.13715 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!