Hypocomplementemic urticarial vasculitis syndrome (HUVS) is an uncommon immune complex-mediated entity characterized by urticaria with persistent acquired hypocomplementemia. First described in 1973, HUVS is associated with several systemic fi ndings including leukocytoclastic vasculitis, severe ang
β¦ LIBER β¦
Hypocomplementemic urticarial vasculitis syndrome
β Scribed by Luis J. Jara; Carmen Navarro; Gabriela Medina; Olga Vera-Lastra; Miguel A. Saavedra
- Book ID
- 107554108
- Publisher
- Springer
- Year
- 2009
- Tongue
- English
- Weight
- 373 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1523-3774
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## Abstract This article describes a transplant recipient with underlying hypocomplementemic urticarial vasculitis syndrome who expressed persistently EpsteinβBarr virus nuclear antigen 1 (EBNA1) in peripheral blood. The patient received a bilateral lung transplant and was subsequently followed wit
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