Omalizumab does not improve skin lesions in a patient with Hypocomplementemic Urticarial Vasculitis Syndrome

Abstract

Hypocomplementemic urticarial vasculitis syndrome (HUVS) is a rare immune complex- mediated disease being characterized by persistent urticarial lesions, hypocomplementemia and possible organ involvement [1]. Therapy of HUVS is reported to be challenging [2]. We report on a 36 year old non atopic female who first presented in our university allergy centre with 18 months history of recurrent urticarial flares.

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