IgA Vasculitis

Overview

A systemic non-thrombocytopenic purpura caused by HYPERSENSITIVITY VASCULITIS and deposition of IGA-containing IMMUNE COMPLEXES within the blood vessels throughout the body, including those in the kidney (KIDNEY GLOMERULUS). Clinical symptoms include URTICARIA; ERYTHEMA; ARTHRITIS; GASTROINTESTINAL HEMORRHAGE; and renal involvement. Most cases are seen in children after acute upper respiratory infections.

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about IgA Vasculitis

Topic type

Condition

Category

Dermatology

MeSH classification

C14.907.940.777|C15.378.100.802.375|C15.378.463.515.580|C17.800.862.329|C20.543.520.600|C23.550.414.950.375|C23.888.885.687.375

Preparing for an appointment about IgA Vasculitis

If you are speaking with a healthcare professional about IgA Vasculitis, it can help to prepare a few details in advance.

• Write down your symptoms and when they started.
• Bring details of any medicines, supplements or previous treatments.
• Ask what tests or assessments may be needed.
• Ask what treatment or management options may be suitable.
• Ask when you should seek urgent medical help or follow-up care.

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