Case Report

Polyarteritis Nodosa Complicated by Antiphospholipid Syndrome

Polyarteritis nodosa is a necrotizing vasculitis of small and medium-sized arteries that spares the smallest blood vessels (arterioles, venules, and capillaries). Antiphospholipid syndrome is an autoimmune disorder characterized by venous or arterial thrombosis and/or by fetal losses, associated with antiphospholipid antibodies. The association of both diseases is infrequent. This case…

Posted in: anticardiolipin antibodies 2 antiphospholipid syndrome 2 polyarteritis nodosa 3

Expired CME Article

Antiphospholipid Syndrome: Review

Antiphospholipid syndrome spans many medical disciplines. Classic criteria include the presence of anticardiolipin antibody or lupus anticoagulant with typical complications of thrombosis or pregnancy loss. Other common associated manifestations include livedo reticularis, thrombocytopenia, valvular heart disease, and nephropathy with renal insufficiency, hypertension, and proteinuria. Treatment of serious complications with anticoagulation…

Posted in: antiphospholipid syndrome 2 thrombosis 4
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