Cases of catastrophic anti-phospholipid syndrome in systemic lupus erythematosus: An experience

Author:

Hegde Arun1,Dorji Thinley23ORCID,Asturkar Vikram4,Yangzom Sonam56,Bhanu Kovilapu Uday6

Affiliation:

1. Department of Rheumatology, Command Hospital (Southern Command), Pune, India

2. Department of Internal Medicine, Jigme Dorji Wangchuck National Referral Hospital, Thimphu, Bhutan

3. Department of Internal Medicine, Armed Forces Medical College, Pune, India

4. Department of Neurology, Command Hospital (Southern Command), Pune, India

5. Department of Radiodiagnosis and Imaging, Jigme Dorji Wangchuck National Referral Hospital, Thimphu, Bhutan

6. Department of Radiodiagnosis and Imaging, Armed Forces Medical College, Pune, India

Abstract

Anti-phospholipid syndrome is an autoimmune disorder characterized by episodes of arterial and/or venous thrombosis and/or pregnancy morbidity in the presence of anti-phospholipid antibodies. Catastrophic anti-phospholipid syndrome is an accelerated form of the disease with rapid involvement of multiple organ systems often posing a diagnostic challenge. There is a paucity of literature on the myriad presentations of catastrophic anti-phospholipid syndrome owing to the orphan nature of the disease. We present three cases of catastrophic anti-phospholipid syndrome in patients with systemic lupus erythematosus that presented with episodes of thrombosis involving both arterial and venous systems and multisystem organ failure. Timely diagnoses were made based on a high index of suspicion and were managed with a combination of systemic glucocorticoids, cyclophosphamide, plasmapheresis, intravenous immunoglobulin and other supportive measures. However, despite providing the standard of care, we encountered a poor outcome in two of these patients, highlighting the high mortality associated with catastrophic anti-phospholipid syndrome.

Publisher

SAGE Publications

Subject

General Medicine

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