Vascular Endothelial Cell Function in Catastrophic Antiphospholipid Syndrome: A Case Report and Review of the Literature

Catastrophic antiphospholipid syndrome (CAPS) is a rare autoimmune condition, which has been associated with a high mortality rate. However, with current management that includes a combination of anticoagulation, glucocorticoid administration, and plasma exchange, mortality rate has declined. Despit...

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Main Authors: B. Routy, T. Huynh, R. Fraser, C. Séguin
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:Case Reports in Hematology
Online Access:http://dx.doi.org/10.1155/2013/710365
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spelling doaj-442f967e2058466c803a234ad8d037432020-11-25T00:09:18ZengHindawi LimitedCase Reports in Hematology2090-65602090-65792013-01-01201310.1155/2013/710365710365Vascular Endothelial Cell Function in Catastrophic Antiphospholipid Syndrome: A Case Report and Review of the LiteratureB. Routy0T. Huynh1R. Fraser2C. Séguin3Division of Haematology, Department of Medicine, McGill University Health Center (MUHC), 1650 Cedar Avenue, Montreal, QC, H3G 1A4, CanadaDivision of Cardiology, Department of Medicine, McGill University Health Center (MUHC), 1650 Cedar Avenue, Montreal, QC, H3G 1A4, CanadaDepartment of Pathology, McGill University Health Center (MUHC), 1650 Cedar Avenue, Montreal, QC, H3G 1A4, CanadaDivision of Haematology, Department of Medicine, McGill University Health Center (MUHC), 1650 Cedar Avenue, Montreal, QC, H3G 1A4, CanadaCatastrophic antiphospholipid syndrome (CAPS) is a rare autoimmune condition, which has been associated with a high mortality rate. However, with current management that includes a combination of anticoagulation, glucocorticoid administration, and plasma exchange, mortality rate has declined. Despite survival improvement with new generation immunosuppressive agents, their mechanisms of action are poorly defined, and CAPS is still considered a high-risk complication in patients known with antiphospholipid antibody syndrome. Herein, we present a case of a 79-year-old male who presented with a myocardial infarct and renal failure secondary to CAPS following a splenectomy for immune thrombocytopenia. Regardless of rapid combination of first-line treatment and rituximab therapy, the patient developed lethal cardiogenic shock secondary to mitral valve papillary muscle necrosis. Discussion of the pathophysiology and avenues of future therapies in CAPS are reported.http://dx.doi.org/10.1155/2013/710365
collection DOAJ
language English
format Article
sources DOAJ
author B. Routy
T. Huynh
R. Fraser
C. Séguin
spellingShingle B. Routy
T. Huynh
R. Fraser
C. Séguin
Vascular Endothelial Cell Function in Catastrophic Antiphospholipid Syndrome: A Case Report and Review of the Literature
Case Reports in Hematology
author_facet B. Routy
T. Huynh
R. Fraser
C. Séguin
author_sort B. Routy
title Vascular Endothelial Cell Function in Catastrophic Antiphospholipid Syndrome: A Case Report and Review of the Literature
title_short Vascular Endothelial Cell Function in Catastrophic Antiphospholipid Syndrome: A Case Report and Review of the Literature
title_full Vascular Endothelial Cell Function in Catastrophic Antiphospholipid Syndrome: A Case Report and Review of the Literature
title_fullStr Vascular Endothelial Cell Function in Catastrophic Antiphospholipid Syndrome: A Case Report and Review of the Literature
title_full_unstemmed Vascular Endothelial Cell Function in Catastrophic Antiphospholipid Syndrome: A Case Report and Review of the Literature
title_sort vascular endothelial cell function in catastrophic antiphospholipid syndrome: a case report and review of the literature
publisher Hindawi Limited
series Case Reports in Hematology
issn 2090-6560
2090-6579
publishDate 2013-01-01
description Catastrophic antiphospholipid syndrome (CAPS) is a rare autoimmune condition, which has been associated with a high mortality rate. However, with current management that includes a combination of anticoagulation, glucocorticoid administration, and plasma exchange, mortality rate has declined. Despite survival improvement with new generation immunosuppressive agents, their mechanisms of action are poorly defined, and CAPS is still considered a high-risk complication in patients known with antiphospholipid antibody syndrome. Herein, we present a case of a 79-year-old male who presented with a myocardial infarct and renal failure secondary to CAPS following a splenectomy for immune thrombocytopenia. Regardless of rapid combination of first-line treatment and rituximab therapy, the patient developed lethal cardiogenic shock secondary to mitral valve papillary muscle necrosis. Discussion of the pathophysiology and avenues of future therapies in CAPS are reported.
url http://dx.doi.org/10.1155/2013/710365
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