Acute dilated cardiomyopathy in the setting of catastrophic antiphospholipid syndrome and thrombotic microangiopathy: A case series and review. Issue 1 (31st July 2020)
- Record Type:
- Journal Article
- Title:
- Acute dilated cardiomyopathy in the setting of catastrophic antiphospholipid syndrome and thrombotic microangiopathy: A case series and review. Issue 1 (31st July 2020)
- Main Title:
- Acute dilated cardiomyopathy in the setting of catastrophic antiphospholipid syndrome and thrombotic microangiopathy: A case series and review
- Authors:
- Hermel, Melody
Hermel, David
Azam, Saif
Shinbane, Jerold
Sarcon, Annahita
Jones, Erika
Mehta, Arjun
Grazette, Luanda
Liebman, Howard
Weitz, Ilene - Abstract:
- Abstract: Catastrophic antiphospholipid antibody syndrome (CAPS) is a rare form of antiphospholipid syndrome, an autoimmune condition characterized by vascular thromboses, pregnancy loss, and antiphospholipid (aPL) antibodies. Diagnosis of CAPS relies on thrombosis of at least three different organs systems over 1 week, histopathological evidence of small vessel occlusion, and high aPL antibody titers. In a subset of precipitating circumstances, activation or disruption of endothelial cells in the microvasculature may occur along with cardiomyopathy. We present two cases of CAPS‐associated dilated cardiomyopathy at our institution, focusing on disease management, pathophysiology, and treatment. These patients were of Southeastern Asian descent, raising the possibility of genetic polymorphisms contributing to the development of cardiomyopathy. Both met CAPS criteria and both demonstrated clinicopathologic thrombotic microangiopathy (TMA) and complement activation and developed severe dilated cardiomyopathy with shock. Complement activation plays an important role in the development of CAPS and may be important in the pathogenesis of CAPS‐associated cardiomyopathy. Clinical suspicion for TMA as a pathophysiologic mechanism of unexplained heart failure in CAPS is important and increased awareness of cardiac side effects is necessary so that early treatment can be initiated to halt further cardiac and systemic complications.
- Is Part Of:
- EJHaem. Volume 1:Issue 1(2020)
- Journal:
- EJHaem
- Issue:
- Volume 1:Issue 1(2020)
- Issue Display:
- Volume 1, Issue 1 (2020)
- Year:
- 2020
- Volume:
- 1
- Issue:
- 1
- Issue Sort Value:
- 2020-0001-0001-0000
- Page Start:
- 44
- Page End:
- 50
- Publication Date:
- 2020-07-31
- Subjects:
- atypical hemolytic uremic syndrome -- cardiomyopathy -- catastrophic antiphospholipid antibody syndrome -- complement -- thrombotic microangiopathy
Hematology -- Periodicals
616.15 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
https://onlinelibrary.wiley.com/journal/26886146 ↗ - DOI:
- 10.1002/jha2.71 ↗
- Languages:
- English
- ISSNs:
- 2688-6146
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14751.xml