Henoch-Schönlein purpura (IgA vasculitis)
IgA-mediated small-vessel vasculitis (often post-URTI)
Overview
The commonest childhood vasculitis — IgA immune complexes deposit in small vessels. A classic tetrad of palpable purpura, arthralgia, abdominal pain and renal involvement, often after an upper respiratory infection.
Recognise
- Palpable purpura on the buttocks and extensor legs (symmetrical) with NORMAL platelets
- Arthralgia/arthritis (knees, ankles)
- Colicky abdominal pain (risk of intussusception)
- Renal: haematuria/proteinuria (IgA nephropathy spectrum)
Red flags
- Severe abdominal pain (intussusception), GI bleeding, hypertension or significant proteinuria (renal involvement)
Differentials & how to tell them apart
Investigations
Clinical. FBC + film (platelets NORMAL — distinguishes ITP/leukaemia), U&E, urinalysis + BP (renal), coagulation normal; biopsy only if atypical.
Management
Supportive care + BP/urinalysis monitoring for renal involvement
- 1Supportive: analgesia, hydration, rest. Check BP and urinalysis to detect renal involvement.Gate: Severe abdominal pain → exclude intussusception (HSP causes the ileo-ileal type); significant proteinuria/AKI → nephrology
- 2Monitor urine/BP for weeks–months (nephritis can be delayed); steroids for severe disease.
Key points
Platelets are NORMAL in HSP (a vasculitis, not thrombocytopenia) — the key split from ITP. Renal follow-up matters because nephritis can appear late.
Monitor & prognosis
Serial BP + urinalysis for 6–12 months (delayed nephritis).
Usually self-limiting; renal involvement determines long-term outcome.
Source: NICE CKS Henoch-Schönlein purpura; RCPCH