Behçet's disease is a systemic vasculitis of unknown aetiology that may involve veins and arteries of all sizes. It occurs most commonly in the second or third decades of life and it is characterised by recurrent oral and genital ulceration and chronic relapsing uveitis. We present here a case of Behçet's disease complicated by an inflammatory aortitis successfully treated with infliximab and endovascular stenting. © M.A. Lee et al., 2012.
CITATION STYLE
Lee, M. A., Kyle, S., & Moots, R. J. (2012). The successful treatment of inflammatory aortitis in Behçet’s disease with infliximab and endovascular intra-aortic stenting. Rheumatology Reports, 4(1), 4–5. https://doi.org/10.4081/rr.2012.e2
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