Púrpura de Henoch-Schonlein diagnóstico por biopsia renal: reporte de caso

Abstract

Henoch-Schönlein Purpura is an inflammatory disease characterized by deposits of immunoglobulin A (IgA) in the walls of blood vessels, producing a series of symptoms that mainly affect the skin, joints, gastrointestinal system and kidneys. The exact cause is not completely known, but it is believed that there is an autoimmune component as well as a genetic predisposition. It affects children more frequently than adults. Larger studies are required to evaluate the effectiveness of corticosteroids and possibly develop an approach that includes guidelines for symptomatic treatment, immunosuppression, and immunomodulation.