scholarly journals A case report of systemic lupus erythematosus with hypocomplementemic urticarial vasculitis syndrome.

1989 ◽  
Vol 12 (2) ◽  
pp. 238-244
Author(s):  
Masahiro Yamamura ◽  
Koji Nishiya ◽  
Tetsuki Amano ◽  
Shinya Suzuki ◽  
Zensuke Ota
2015 ◽  
Vol 2015 ◽  
pp. 1-3 ◽  
Author(s):  
Misbah Nasheela Ghazanfar ◽  
Simon Francis Thomsen

Urticarial vasculitis is characterised by inflamed itching or burning red patches or wheals that resemble urticaria but persist for greater than 24 hours. It is often idiopathic but is sometimes associated with collagen-vascular disease, particularly systemic lupus erythematosus. Treatment options include oral antihistamines, oral corticosteroids, dapsone, colchicine or hydroxychloroquine. We describe a male patient with urticarial vasculitis who was treated with omalizumab (anti-IgE) with convincing results and provide a review of previous reports of patients with urticarial vasculitis treated with omalizumab.


1999 ◽  
Vol 34 (4) ◽  
pp. 745-751 ◽  
Author(s):  
Marten Trendelenburg ◽  
Salome Courvoisier ◽  
Peter J. Späth ◽  
Solange Moll ◽  
Michael Mihatsch ◽  
...  

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