Abstract | BACKGROUND: Hypocomplementemic urticarial vasculitis, described by MacDuffie in 1973, is rare. Some doubt surrounds its classification. We report a case of hypocomplementemic urticarial vasculitis (MacDuffie syndrome) treated with dapsone with a favorable outcome. CASE REPORT: Over a number of years, a 43-year-old man presented urticarial vasculitis attacks with palpebral oedema and systemic symptoms such as fever and arthralgia. In 2006, MacDuffie syndrome was diagnosed on the grounds of positive anti-C1q antibodies. Treatment with dapsone was started and resulted in considerable improvement. DISCUSSION:
|
Authors | M Hérault, J Mazet, P Beurey, J-F Cuny, A Barbaud, J-L Schmutz, A-C Bursztejn |
Journal | Annales de dermatologie et de venereologie
(Ann Dermatol Venereol)
2010 Aug-Sep
Vol. 137
Issue 8-9
Pg. 541-5
ISSN: 0151-9638 [Print] France |
Vernacular Title | Une vascularite hypocomplémentémique traitée par dapsone. |
PMID | 20804899
(Publication Type: Case Reports, English Abstract, Journal Article)
|
Copyright | Copyright 2010 Elsevier Masson SAS. All rights reserved. |
Chemical References |
- Autoantibodies
- Complement C1q
- Dapsone
- Complement System Proteins
|
Topics |
- Adult
- Autoantibodies
(blood, immunology)
- Complement C1q
(immunology)
- Complement System Proteins
(deficiency)
- Dapsone
(therapeutic use)
- Diagnosis, Differential
- Humans
- Lupus Erythematosus, Systemic
(diagnosis)
- Male
- Remission Induction
- Urticaria
(blood, drug therapy, immunology)
- Vasculitis, Leukocytoclastic, Cutaneous
(blood, diagnosis, drug therapy, immunology)
|