Key result
Triple-positive antiphospholipid syndrome on rivaroxaban presents with extensive native aortic valve thrombosis across all three cusps.
Why the study?
Native aortic valve thrombosis is an uncommon source of systemic thromboembolism that presents a diagnostic challenge because of overlap with infective endocarditis, nonbacterial thrombotic endocarditis, and other valvular masses.
Case Report (n=1)
This case report highlights the risk of extensive native aortic valve thrombosis and recurrent thromboembolism despite rivaroxaban therapy in a patient with suspected high-risk triple-positive antiphospholipid syndrome.
Answers are grounded in this paper and cite their sources.
Valve thrombosis may occur in high-risk APS on rivaroxaban; leaves open optimal anticoagulation and diagnostic differentiation of valvular masses.
Native aortic valve (AoV) thrombosis is an uncommon but clinically important source of systemic thromboembolism.1,2 Its presentation as a valvular mass can create a diagnostic challenge because of overlap with infective endocarditis, nonbacterial thrombotic endocarditis (NBTE), and other valvular masses. We report extensive native AoV thrombosis involving all 3 cusps, with predominant involvement of the noncoronary cusp (NCC), in a patient with recurrent arterial and venous thromboembolism despite rivaroxaban therapy and triple-positive antiphospholipid antibody testing strongly suggestive of high-risk antiphospholipid syndrome (APS).
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Abid et al. (2026) conducted a case report in Native aortic valve thrombosis and suspected high-risk antiphospholipid syndrome (n=1). Triple-positive antiphospholipid syndrome on rivaroxaban therapy was evaluated on Extensive native aortic valve thrombosis involving all 3 cusps. Suspected triple-positive antiphospholipid syndrome on rivaroxaban presented with extensive native aortic valve thrombosis involving all 3 cusps in 1 patient with recurrent thromboembolism.
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