Polycythemia Vera and Mesenteric Arterial Thrombosis

Abstract

Recurrent mesenteric arterial thrombosis developed in a 56-year-old man with polycythemia vera (PV) despite therapy with heparin sodium, warfarin sodium, and standard doses of aspirin and dipyridamole. Platelet aggregation studies disclosed a normal response to aggregating agents in the presence of blood levels of aspirin that usually inhibit in vitro platelet aggregation. Increasing the in vivo dose of aspirin was associated with inhibition of in vitro platelet aggregation and, thereafter, arterial thrombosis did not recur. This case demonstrates that some patients with PV and arterial thrombosis may be refractory to standard doses of anticoagulants and platelet antiaggregating agents.