Development of Henoch-Schönlein purpura in a patient with Behçet's disease presenting with recurrent deep vein thrombosis.

Abstract

Behçet's disease (BD) is a multisystemic vasculitis. Here we report a case of association with BD and Henoch-Schönlein purpura (HSP). He was diagnosed as having BD with oral ulcer, genital ulcer, papular skin lesion, deep vein thrombosis (DVT) and positive pathergy reaction. Ascending venograms of both legs showed segmental occlusion from both superficial femoral vein (SFV) to inferior vena cava (IVC) with intravascular thrombus. He developed abdominal pain, bloody diarrhea, microscopic hematuria, and widespread palpable purpura on both legs, compatible with HSP. Histologic examination of the skin lesion confirmed cutaneous leukocytoclastic vasculitis with IgA-containing immune deposits. The HSP-like manifestations markedly improved with high-dose steroid therapy.

• Authors: Y-W Park, J-J Park, J-B Lee, S-S Lee
• Journal: Clinical and experimental rheumatology (Clin Exp Rheumatol) 2007 Jul-Aug Vol. 25 Issue 4 Suppl 45 Pg. S96-8 ISSN: 0392-856X [Print] Italy
• PMID: 17949560 (Publication Type: Case Reports, Journal Article)

Chemical References

• Anti-Inflammatory Agents
• Prednisolone

Topics

• Adult
• Anti-Inflammatory Agents (therapeutic use)
• Behcet Syndrome (complications)
• Humans
• IgA Vasculitis (complications, drug therapy, pathology)
• Male
• Prednisolone (therapeutic use)
• Venous Thrombosis (complications)