Pediatric vasculitis encompasses a diverse group of rare autoimmune diseases characterized by inflammation of blood vessels. While vasculitis can affect individuals of any age, its presentation, diagnosis, and management in pediatric patients pose unique challenges. This article aims to explore these distinctive aspects, shedding light on the complexities of diagnosing and managing vasculitis in children. Vasculitis in children encompasses a spectrum of diseases, including but not limited to Kawasaki disease, Henoch-Schönlein purpura, polyarteritis nodosa, and granulomatosis with polyangiitis. These diseases vary in their clinical presentation, affected vessel size, and associated systemic manifestations. For instance, Kawasaki disease predominantly affects medium-sized vessels, presenting with fever, mucocutaneous involvement, and coronary artery abnormalities, while Henoch-Schönlein purpura typically involves small vessels, manifesting as palpable purpura, joint pain, abdominal pain, and renal involvement.
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Journal of Vasculitis received 83 citations as per Google Scholar report
