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Henoch-Schonlein Purpura

Henoch-Schonlein Purpura

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Pathology:

Small vessel vasculitis characterised by deposition of immunoglobulin A (IgA) in both the skin and kidneys.

Aetiology:

Henoch-Schonlein purpura (HSP) is much more common in young males and often follows an upper respiratory tract infection (URTI).

Symptoms:

  • Abdominal pain
  • Haematuria
  • Musculoskeletal pain
  • Rash

Signs:

  • Purpura on the legs and buttocks
  • Arthralgia
  • Abdominal pain
  • Gastrointestinal (GI) haemorrhage (often due to intussusception)
  • Haematuria

Investigations:

  • Bloods: Raised IgA, erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP); full blood count (FBC) shows a raised platelet count.
  • Skin biopsy: IgA and complement 3 (C3) in the blood vessel wall.

Treatment:

  • Conservative: Spontaneous recovery occurs within 4 weeks.
  • Medical: Analgesia for arthralgia.

Complications:

Long-term complications are secondary to renal involvement and require follow-up for up to one year to monitor renal function and blood pressure.

Prognosis:

Excellent.

Rectangle: Rounded Corners: NOTE FOR PUBLISHERS –     Image of Purpuric Rash associated with Henoch-Schonlein Purpura

 

Figure 8.5 Henoch-Schonlein Purpura

 

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