Severe hemorrhagic bullous lesions in Henoch Schonlein purpura: three pediatric cases and review of the literature

Sandra Trapani (1) , Paola Mariotti (1, 2) , Massimo Resti (1) , Lido Nappini (1, 3) , Maurizio Martino (1) , Fernanda Falcini (1)

1 Department of Pediatrics
2 Division of Pediatrics
3 Division of Pediatrics

Henoch Schonlein purpura (HSP) is a small-sized blood vessels vasculitis, resulting from immunoglobulin A-mediated inflammation. It is the most common acute systemic vasculitis in childhood and mainly affects skin, gastrointestinal tract, joints and kidney. Skin lesions, usually presenting as erythematous maculopapules, petechiae, and purpura, often involve lower extremities and buttocks, but may also extend to the upper extremities, face and trunk. Conversely to adults, hemorrhagic bullous evolution has been seldom described in childhood. The pressure is likely a factor into the pathogenesis of bullae. We report on three new pediatric cases of HSP with hemorrhagic bullous skin lesions, and a review of the literature. Bullous evolution represents an unusual, but well-recognized cutaneous manifestation that may be a source of diagnostic dilemma, but does not seem to have any prognostic value in the outcome of HSP.

Mots clés: Bullous Henoch Schonlein purpura; Childhood vasculitis

Sandra Trapani, Paola Mariotti, Massimo Resti, Lido Nappini, Maurizio Martino, et al.. Severe hemorrhagic bullous lesions in Henoch Schonlein purpura: three pediatric cases and review of the literature. Rheumatology International, 2009, 30 (10), pp.1355-1359. ⟨10.1007/s00296-009-1055-8⟩. ⟨hal-00552489⟩