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Young Stroke Following Libman-Sacks Endocarditis associated with Systemic Lupus Erythematosus and Secondary Antiphospholipid Antibody Syndrome Cover

Young Stroke Following Libman-Sacks Endocarditis associated with Systemic Lupus Erythematosus and Secondary Antiphospholipid Antibody Syndrome

Open Access
|Dec 2022

Abstract

Libman-Sacks Endocarditis (LSE) is a form of nonbacterial thrombotic endocarditis (NBTE) occurring in the set­ting of hypercoagulable states like solid organ malignancies, systemic lupus erythematosus (SLE) and primary or secondary antiphospholipid antibody syndrome (APLS).LSE is the most characteristic cardiac manifestation of SLE. Even though the incidence of clinically significant valve dysfunction and embolic phenomenon is low when it is associated with secondary APLS, risk for embolic cerebrovascular events is high.

We present a case of a 39-year-old female who admitted with a left sided ischemic stroke ultimately turned out to be having LSE secondary to SLE and APLS. This will demonstrate the importance of having a high degree of suspicion for the diagnosis of LSE and its etiology when evaluating a young patient with stroke.

Language: English
Page range: 45 - 47
Published on: Dec 23, 2022
Published by: Ruhunu Clinical Society
In partnership with: Paradigm Publishing Services

© 2022 Amanda Amarasingha, published by Ruhunu Clinical Society
This work is licensed under the Creative Commons Attribution 4.0 License.