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Updated: Jan 16, 2026

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
[Hypocomplementemic urticarial vasculitis in SLE: between urticaria and autoimmunity].
Jacqueline Edith Mut Quej1, Paula Isabel Ramirez Molina2, Maria Isabel Saad Manzanera2
1Unidad Médica de Alta Especialdad, Hospital de Especialidades, Centro Médico Nacional Siglo XXI, Intituto Mexicano del Seguro Social, Ciudad de México. jacquelinemut18@gmail.com.
Hypocomplementemic urticarial vasculitis (HUV) is crucial to consider in systemic lupus erythematosus (SLE) patients with persistent skin lesions. Early diagnosis and management of HUV are vital to prevent systemic complications.
Area of Science:
- Dermatology
- Rheumatology
- Immunology
Background:
- Urticarial vasculitis (UV) affects small blood vessels, presenting as persistent urticarial lesions (>24 hours) with leukocytoclastic vasculitis.
- UV is classified into normocomplementemic (NUV) and hypocomplementemic (HUV) types, with HUV linked to systemic diseases like SLE.
- The incidence of UV is approximately 0.5 per 100,000 person-years.
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