Multisystemic manifestations of IgA vasculitis.

摘要: Immunoglobulin A vasculitis (IgAV), also known as Henoch-Schonlein Purpura, is one of the most common kind systemic in children, and due to involvement small blood vessels throughout body, this disease can cause a variety symptoms different organs. Our aim was review data on various manifestations IgAV. research literature performed PubMed database, utilizing MeSH terms "IgA vasculitis" "Henoch Schonlein Purpura". According predetermined structure manuscript, we extracted sorted out relevant data. Clinically, almost all patients will present with palpable skin purpura, together arthritis, gastrointestinal tract involvement, or kidney damage. Other rare include neurological symptoms, scrotal cardiopulmonary disease. When uncommon complications occur, may be misdiagnosed other diseases, thus delaying treatment. Although course IgAV mostly self-limited, misdiagnosis lead poor prognosis. comprehensive awareness clinical necessary prerequisite for its timely diagnosis. Prompt diagnosis adequate treatment are essential optimal results.