Managing Behçet's disease: An update on current and emerging treatment options.

Abstract:

:Behçet's disease is an autoinflammatory vasculitis of unknown origin characterized by recurrent oral and genital ulcers, uveitis, arthritis and skin lesions. Additionally, involvement of the gastrointestinal tract, central nervous system and large vessels may occur. The disease is prevalent in countries along the ancient Silk Road from Eastern Asia to the Mediterranean Basin. Many treatment modalities are currently available. The choice of treatment depends on organ involvement and severity of disease. Topical treatment with corticosteroids is often sufficient for mucocutaneous involvement, however for more severe disease with vasculitis or neurological involvement a more aggressive approach is warranted. Newer drugs (biologicals) influencing cytokines and thereby T-cell function are promising with an acceptable side effect profile. Unfortunately, reimbursement of the costs of biologicals for rare disease is still a problem in various countries. In this report we discuss the current treatment modalities for Behçet's disease.

journal_name

Ther Clin Risk Manag

authors

van Daele PL,Kappen JH,van Hagen PM,van Laar JA

doi

10.2147/tcrm.s4446

subject

Has Abstract

pub_date

2009-04-01 00:00:00

pages

385-90

issue

2

eissn

1176-6336

issn

1178-203X

journal_volume

5

pub_type

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