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Updated: Jul 15, 2026

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
[Hypocomplementemic urticarial vasculitis syndrome. Successful therapy with intravenous immunoglobulins]
P Staubach-Renz1, E von Stebut, W Bräuninger
1Universitäts-Hautklinik Mainz, Langenbeckstrasse 1, 55101 Mainz, Deutschland. staubach@hautklinik.klinik.uni-mainz.de
Abstract:
Autoimmune diseases can initially present as chronic urticaria. We describe the course of a patient with hypocomplementemic urticarial vasculitis syndrome (HUVS) as well as his successful treatment with high-dose intravenous immunoglobulins (IVIG). HUVS was diagnosed clinically and confirmed by histology and laboratory studies. After only one cycle with IVIG (2 g/kg) all HUVS symptoms were significantly decreased.
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