December 2025 Br J Cardiol 2025;32(4) doi:10.5837/bjc.2025.054 Online First
Simão Carvalho, Diana Carvalho, Inês Cruz, Tiago Aguiar, Carlos Costa, Raquel Ferreira, Andreia Fernandes, Ana Briosa Neves
Introduction Systemic inflammatory diseases (SIDs) are syndromes characterised by constitutional symptoms and multi-organ involvement. Cardiac manifestations are rare but often indicate a poor prognosis.1 Behçet’s disease is a relapsing inflammatory condition presenting with recurrent aphthous stomatitis, genital ulcers, and uveitis. Cardiac involvement occurs in 1–5% of cases and includes myocarditis, conduction abnormalities, and intracardiac thrombi.2 Antiphospholipid syndrome (APS) is an autoimmune disorder associated with thrombotic events and recurrent pregnancy loss. Its cardiac manifestations range from accelerated atherosclerosi
You need to be a member to print this page.
Find out more about our membership benefits
You need to be a member to download PDF's.
Find out more about our membership benefits