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Rev. Assoc. Med. Bras. (1992) ; 65(6): 772-774, June 2019.
Artículo en Inglés | LILACS | ID: biblio-1041042

RESUMEN

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.


Asunto(s)
Humanos , Femenino , Anciano , Accidente Cerebrovascular/etiología , Trombocitemia Esencial/complicaciones , Factores de Riesgo , Accidente Cerebrovascular/genética , Janus Quinasa 2/genética , Trombocitemia Esencial/genética , Mutación
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