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Haemorrhagic bullous lesions in a 3-year-old girl with Henoch–Schölein purpura

Authors


Jun Ho Lee, MD, Department of Pediatrics, CHA Bundang Medical Center, CHA University, 351 Yatap-dong, Bundang-gu, Seongnam-si, Gyeonggi-do 463-712, Korea.
Tel: +82-10-3180-6511 |
Fax: +82-31-780-5011 |
Email: naesusana@yahoo.co.kr

Abstract

Henoch–Schönlein purpura (HSP) is the most common vasculitis in children and is characterized by cutaneous purpura, arthritis, abdominal pain and nephritis. We report a case involving a 3-year-old girl with HSP who displayed rapidly evolving haemorrhagic bullae from primary purpuric lesions during systemic corticosteroid therapy.

Conclusion:  The bullae disappeared within 7 days of systemic corticosteroid therapy, although some scarring of the skin occurred. Also, bullae should not be considered as a poor prognostic factor of renal outcome in HSP.

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