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.
journal_name
Clin Exp Rheumatoljournal_title
Clinical and experimental rheumatologyauthors
Park YW,Park JJ,Lee JB,Lee SSsubject
Has Abstractpub_date
2007-07-01 00:00:00pages
S96-8issue
4 Suppl 45eissn
0392-856Xissn
1593-098Xpii
2135journal_volume
25pub_type
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journal_title：Clinical and experimental rheumatology
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journal_title：Clinical and experimental rheumatology
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pub_type： 杂志文章
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