Libman-Sacks endocarditis in a Bangladeshi patient suffering from rhupus

Shahana Zaman1, Muhammad Abdur Rahim2, Lima Asrin Sayami1

  • 1Junior Consultant, Department of Cardiology, National Institute of Cardiovascular Diseases (NICVD), Dhaka, Bangladesh.

Tropical Doctor
|June 11, 2019
PubMed

Insights

Libman-Sacks endocarditis, a cardiac condition in systemic lupus erythematosus, is rarely associated with rhupus. This case highlights a patient with rhupus and Libman-Sacks endocarditis who tested negative for anti-phospholipid antibodies.

Area of Science:

  • Cardiology
  • Rheumatology
  • Immunology

Background:

  • Libman-Sacks endocarditis (LSE) is a characteristic cardiac manifestation of systemic lupus erythematosus (SLE).
  • Symptomatic patients with LSE often experience systemic emboli, frequently associated with anti-phospholipid antibodies (aPA).
  • The co-occurrence of LSE with rheumatoid arthritis (RA) and lupus, termed 'rhupus', is exceptionally rare.

Observation:

  • This report details a rare case of a patient diagnosed with RA seven years prior.
  • The patient had a history of an acute ischemic stroke one year before this evaluation.
  • Echocardiography revealed evidence of LSE during routine assessment.

Findings:

  • The patient presented with echocardiographic findings consistent with LSE.
  • Despite the presence of LSE and a history of stroke, the patient tested negative for aPA.
  • This case represents a rare instance of LSE in a patient with rhupus, lacking the typical aPA association.

Implications:

  • This case expands the understanding of LSE presentation in autoimmune overlap syndromes.
  • It suggests that LSE can occur in rhupus patients even without detectable anti-phospholipid antibodies.
  • Further research may be needed to elucidate the specific pathogenic mechanisms of LSE in aPA-negative rhupus patients.

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