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Rev. Assoc. Med. Bras. (1992) ; 65(6): 772-774, June 2019.
Artigo em Inglês | LILACS | ID: biblio-1041042

RESUMO

SUMMARY The essential thrombocythemia is one of the seven described forms of myeloproliferative neoplasms. It is characterized by megakaryocytic hyperplasia with consequent thrombocytosis maintained in the peripheral blood, favoring the occurrence of thrombo-hemorrhagic phenomena. We present the case of an 81-year-old woman with a history of ischemic stroke in the context of a sustained thrombocytosis, which led to a spinal study and a search for the V617F mutation in the JAK2 gene, which was positive. The patient started cytoreductive therapy with hydroxyurea with favorable current evolution.


Assuntos
Humanos , Feminino , Idoso , Acidente Vascular Cerebral/etiologia , Trombocitemia Essencial/complicações , Fatores de Risco , Acidente Vascular Cerebral/genética , Janus Quinase 2/genética , Trombocitemia Essencial/genética , Mutação
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