Abstract
Thoracic aortic mural thrombus (TAMT) is a rare pathology and potential source of cerebral, visceral, and peripheral emboli. We present a 62-year-old male in a hypercoagulable state due to primary polycythemia vera (PV) developed TAMT and catastrophic thromboembolisms despite aggressive medical and surgical management. The outcomes and adverse events of endovascular exclusion of TAMT in the presence of PV are unknown. We would recommend proceeding with extreme caution when performing endovascular exclusion of TAMT, as PV may be a prohibitive risk.
| Original language | English |
|---|---|
| Pages (from-to) | 89-92 |
| Number of pages | 4 |
| Journal | Vascular |
| Volume | 23 |
| Issue number | 1 |
| DOIs | |
| State | Published - Feb 17 2015 |
Bibliographical note
Publisher Copyright:© The Author(s) 2014 Reprints and permissions: sagepub.co.uk/journalsPermissions.nav.
Keywords
- endovascular aortic repair
- polycythemia vera
- Thoracic aortic mural thrombus
ASJC Scopus subject areas
- Surgery
- Radiology Nuclear Medicine and imaging
- Cardiology and Cardiovascular Medicine