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Antiphospholipid antibody associated thrombocytopenia and the paradoxical risk of thrombosisDepartment of Medicine II, Hokkaido University Graduate School of Medicine, Sapporo, Japan, at3tat{at}med.hokudai.ac.jp
Department of Medicine II, Hokkaido University Graduate School of Medicine, Sapporo, Japan
Department of Medicine II, Hokkaido University Graduate School of Medicine, Sapporo, Japan
Department of Medicine II, Hokkaido University Graduate School of Medicine, Sapporo, Japan The pathogenesis of thrombocytopenia in patients with antiphospholipid syndrome (APS) is heterogeneous. Patients with antiphospholipid antibodies (aPL) and thrombocytopenia in the absence of clinical manifestations of APS will be diagnosed and treated as idiopathic thrombocytopenic purpura. However, the presence of aPL places those individuals at particular risk for developing both bleeding and thrombotic complications. Therefore, we propose the inclusion of such patients in the subgroup aPL-associated thrombocytopenia. More attention should be devoted to this subgroup of patients to elucidate the role of aPL in the development of thrombocytopenia and to facilitate the adequate monitoring of its potential thrombotic risk.
Key Words: anticardiolipin antibodies lupus anticoagulant thrombosis
Lupus, Vol. 14, No. 7,
499-504 (2005) This article has been cited by other articles:
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