Ischemic stroke after recombinant factor VIIa treatment in acquired hemophilia A patient
Acquired hemophilia is a rare, life-threatening coagulopathy in adults caused by the development of autoantibodies against factor VIII. Bypass agents such as recombinant factor VIIa (rFVIIa) are usually preferred for bleeding control; however, thromboembolic complications may occur. We report here a...
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Published in | Blood coagulation & fibrinolysis Vol. 23; no. 1; p. 69 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
01.01.2012
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Subjects | |
Online Access | Get more information |
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Summary: | Acquired hemophilia is a rare, life-threatening coagulopathy in adults caused by the development of autoantibodies against factor VIII. Bypass agents such as recombinant factor VIIa (rFVIIa) are usually preferred for bleeding control; however, thromboembolic complications may occur. We report here a case that presented with extensive cutaneous and mucosal bleedings due to factor VIII inhibitors and was treated successfully with rFVIIa and steroid therapy, but was complicated with a life-threatening thromboembolic attack during follow-up. |
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ISSN: | 1473-5733 |
DOI: | 10.1097/MBC.0b013e32834b8267 |