Literature DB >> 17688841

Urticarial vasculitis.

Natalie A Brown1, John D Carter.   

Abstract

Urticarial vasculitis can present in a variety of ways, ranging from a primarily cutaneous disease consisting of chronic urticaria to a lupus-like disease with severe cardiopulmonary disease. Low complement levels and positive anti-C1q antibodies are markers of more severe disease. Care must be taken to look for an underlying condition. The mainstay of therapy is treatment of any underlying condition. Therapies most often employed include corticosteroids, antihistamine, and dapsone, but many others have been utilized.

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Year:  2007        PMID: 17688841     DOI: 10.1007/s11926-007-0050-x

Source DB:  PubMed          Journal:  Curr Rheumatol Rep        ISSN: 1523-3774            Impact factor:   4.686


  35 in total

1.  Atypical fatal hypocomplementemic urticarial vasculitis with involvement of native and homograft aortic valves in an African American man.

Authors:  L Hong; F Wackers; M Dewar; M Kashgarian; P W Askenase
Journal:  J Allergy Clin Immunol       Date:  2000-12       Impact factor: 10.793

2.  Hypocomplementemic urticarial vasculitis and lower cranial nerve palsies.

Authors:  P A Koul; A Wahid; S U Shah; A N Koul; S M Saleem
Journal:  J Assoc Physicians India       Date:  2000-05

3.  Inflammatory myositis complicating hypocomplementemic urticarial vasculitis despite on-going immunosuppression.

Authors:  Gary Y J Chew; Paul A Gatenby
Journal:  Clin Rheumatol       Date:  2006-08-30       Impact factor: 2.980

4.  Hypocomplementaemic urticarial vasculitis: successful treatment with cyclophosphamide-dexamethasone pulse therapy.

Authors:  M Worm; M Muche; P Schulze; W Sterry; G Kolde
Journal:  Br J Dermatol       Date:  1998-10       Impact factor: 9.302

5.  Hypocomplementemia with cutaneous vasculitis and arthritis. Possible immune complex syndrome.

Authors:  F C McDuffie; W M Sams; J E Maldonado; P H Andreini; D L Conn; E A Samayoa
Journal:  Mayo Clin Proc       Date:  1973-05       Impact factor: 7.616

Review 6.  Urticarial vasculitis: a histopathologic and clinical review of 72 cases.

Authors:  D R Mehregan; M J Hall; L E Gibson
Journal:  J Am Acad Dermatol       Date:  1992-03       Impact factor: 11.527

7.  Recurrent angioedema and urticaria.

Authors:  P C Bishop; J J Wisnieski; J Christensen
Journal:  West J Med       Date:  1993-11

8.  Jaccoud's arthritis and panvasculitis in the hypocomplementemic urticarial vasculitis syndrome.

Authors:  A S Sturgess; G O Littlejohn
Journal:  J Rheumatol       Date:  1988       Impact factor: 4.666

9.  Hypocomplementemic urticarial vasculitis syndrome in identical twins.

Authors:  J J Wisnieski; S N Emancipator; N J Korman; J H Lass; T M Zaim; E R McFadden
Journal:  Arthritis Rheum       Date:  1994-07

Review 10.  Urticarial vasculitis and hypocomplementemic urticarial vasculitis syndrome.

Authors:  Mark D P Davis; Jerry D Brewer
Journal:  Immunol Allergy Clin North Am       Date:  2004-05       Impact factor: 3.479

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  1 in total

1.  Juvenile systemic lupus erythematosus and dermatomyositis associated with urticarial vasculitis syndrome: a unique presentation.

Authors:  Patrícia A Macêdo; Carolina B Garcia; Monique K Schmitz; Levi H Jales; Rosa M R Pereira; Jozélio F Carvalho
Journal:  Rheumatol Int       Date:  2010-04-17       Impact factor: 2.631

  1 in total

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