Revisiting Libman-Sacks endocarditis: A historical review and update

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39 Scopus citations

Abstract

Libman-Sacks (LS) endocarditis was first described by Libman and Sacks in 1924, and is characterized by sterile, verrucous valvular lesions with a predisposition for the mitral and aortic valves. It is now regarded as both a cardiac manifestation of systemic lupus erythematosus and, in recent years, of the antiphospholipid syndrome (APS). Though typically mild and asymptomatic, LS endocarditis can lead to significant complications, including severe valvular insufficiency requiring surgery, infective endocarditis, and thromboembolic events, such as stroke and transient ischemic events. Improvements in imaging modalities, particularly in echocardiography, have allowed better estimation of the prevalence of the disease, but further investigation is still needed into its pathogenesis, treatment, and association with APS.

Original languageEnglish (US)
Pages (from-to)126-130
Number of pages5
JournalClinical Reviews in Allergy and Immunology
Volume36
Issue number2-3
DOIs
StatePublished - Jun 2009

Keywords

  • Antiphospholipid syndrome
  • Libman-Sacks endocarditis
  • Systemic lupus erythematosus

ASJC Scopus subject areas

  • Immunology and Allergy

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