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Condition Info
ConditionName
Immunoglobulin A–Associated Vasculitis (IgAV, Henoch-Schonlein purpura)
ConditionDescription
Small vessel vasculitis. Systematic deposition of IgA in different tissue Immunoglobulin A–dominant immune deposits, affecting capillaries, venules, or arterioles; typically involves skin, gut, and glomeruli; associated with arthralgias or arthritis
Symptoms
Generalized abdominal pain; bleeding; Skin: purpura – from the buttocks down Joint: arthralgia (low extremities, large joints) Renal: hematuria Leukoclastic reaction: painless, palpable purpura of buttocks and legs;
PhysicalFindings
Clinical diagnosis; Palpable rush;
ClinicalTests
Clinical diagnosis. UA – microscopic hematuria (not specific), proteinuria PT, PTT; PLATELETS ARE NORNAL; Biopsy – most accurate test but never done (leukocytoclastic vasculitis);
RiskFactors
Children 2-8 years/old; Boys; African-Americans;
IsRedFlag
IsNPLEX
Consequence
Renal insufficiency is not reversible; Nephritic, nephrotic syndrome;
ProgressionFromCondition
Usually follow URI;
TreatmentOptions
Most cases self-limited
PharmOptions
Supportive care (water, NSAIDs); Steroids – severe cases associated with progressive renal insufficiency;
WebLink
https://www.merckmanuals.com/professional/musculoskeletal-and-connective-tissue-disorders/vasculitis/immunoglobulin-a–associated-vasculitis-igav
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