Abstract
Antiphospholipid syndrome (APS) is an acquired thrombophilic disorder characterized by autoantibodies to cell membrane phospholipids. While altered coagulation can complicate end-stage liver disease, there are few reports describing the perioperative management for liver transplantation in recipients with a preexisting hypercoagulable disorder, such as APS. We present a patient with a history of APS, Budd-Chiari syndrome with cirrhosis, hepatopulmonary syndrome, and heparin-induced thrombocytopenia who underwent liver transplantation complicated by hepatic artery thrombosis. Management included postoperative anticoagulation with a factor Xa inhibitor and, after repeat transplantation, transition to long-term anticoagulation therapy with eventual recovery.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 148-150 |
| Number of pages | 3 |
| Journal | A & A case reports |
| Volume | 9 |
| Issue number | 5 |
| DOIs | |
| State | Published - Sep 1 2017 |
ASJC Scopus subject areas
- General Medicine
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