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Rheumatology Advance Access originally published online on April 2, 2007
Rheumatology 2007 46(5):736-741; doi:10.1093/rheumatology/kem034
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© The Author 2007. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org


REVIEWS

Anti-TNF therapy in the management of Behçet's disease—review and basis for recommendations

P. P. Sfikakis, N. Markomichelakis, E. Alpsoy1, S. Assaad-Khalil2, B. Bodaghi3, A. Gul4, S. Ohno5, N. Pipitone6, M. Schirmer7, M. Stanford8, B. Wechsler3, C. Zouboulis9, P. Kaklamanis and H. Yazici4

Athens University, Greece, 1Akdeniz University, Turkey, 2Alexandria University, Egypt, 3Paris IV University, France, 4Istanbul University, Turkey, 5Hokkaido University, Japan, 6Reggio Emilia Hospital, Italy, 7Elizabethenians' Hospital Klagenfurt, Austria, 8King's College, London, UK and 9Dessau Medical Center, Germany.

Correspondence to: P. P. Sfikakis, 18, Ipsilantou Str., Athens, 10676, Greece. E-mail: psfikakis@med.uoa.gr

The first 150 words of the full text of this article appear below.


    Introduction
 
Behçet's disease (BD) is a multisystem, chronic-relapsing, inflammatory disorder classified among the vasculitides [1, 2]. It has a worldwide distribution being more prevalent in the Middle East, Far East and the Mediterranean basin [3]. The diagnosis is entirely based on clinical grounds since no pathognomonic laboratory findings exist. International study group classification criteria used for BD patients participating in research protocols depend on the presence of recurrent oral ulceration plus any two of the following: recurrent genital ulcerations, ocular lesions (anterior or posterior uveitis, or cells in the vitreous on slit lamp examination, or retinal vasculitis), typical skin lesions (erythema nodosum, pseudofollicullitis) and a positive pathergy (skin hyperreactivity) test [4, 5]. The clinical picture of BD is diverse and while recurrent mucocutaneous lesions are usually the only symptoms at the onset of the disease, most patients develop ocular and/or articular, vascular, central . . . [Full Text of this Article]


    Limitations of current therapies and unmet medical needs in Behçet's disease
 

    Anti-TNF agents in Behçet's disease: the current evidence
 
Infliximab
Etanercept
Adalimumab
Safety issues

    Anti-TNF agents in Behçet's disease: recommendations for optimal use
 
Identification of patients likely to benefit from anti-TNF treatment
Selection of anti-TNF agent, monitoring and treatment adjustments
Infliximab for ocular disease

    Anti-TNF agents in Behçet's disease: caution considerations
 

    Summary and conclusions
 

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