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Refractory Heparin-Induced Thrombocytopenia With Cerebral Venous Sinus Thrombosis Treated With IVIg, Steroids, and a Combination of Anticoagulants: A Case Report

dc.contributor.authorGonzales, Mia
dc.contributor.authorPipalia, Amrish
dc.contributor.authorWeil, Andrew
dc.date.accessioned2020-04-21T18:15:58Z
dc.date.available2020-04-21T18:15:58Z
dc.date.issued2019-04-02
dc.description.abstractHeparin-induced thrombocytopenia (HIT) type II is caused by antibody production that bind complexes between heparin and platelet factor 4 leading to platelet consumption and thrombosis. In a small subset of cases referred to as autoimmune HIT, the antibodies activate platelets even in the absence of heparin. Refractory HIT is a type of autoimmune HIT in which thrombocytopenia persists for weeks after heparin discontinuation and carries increased risk for thrombosis and more severe thrombocytopenia. We present a case of refractory HIT with cerebral venous sinus thrombosis (CVST) that was successfully treated with a change in anticoagulant alongside steroids and a second trial of intravenous immunoglobulin (IVIg).en_US
dc.identifier.doi10.1177/2324709619832324
dc.identifier.urihttp://hdl.handle.net/10342/8296
dc.subjectheparin-induced thrombocytopenia, cerebral venous sinus thrombosis, IVIg, refractory HIT, autoimmune HITen_US
dc.titleRefractory Heparin-Induced Thrombocytopenia With Cerebral Venous Sinus Thrombosis Treated With IVIg, Steroids, and a Combination of Anticoagulants: A Case Reporten_US
dc.typeArticleen_US
ecu.journal.nameJournal of Investigative Medicine High Impact Case Reportsen_US
ecu.journal.volume7en_US

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