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Rev. méd. Chile ; 130(1): 79-85, ene. 2002. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-310256

RESUMO

Hereditary hypercoagulability has been identified as risk factor in approximately 30 percent of cerebral venous thrombosis cases. We report three females with this association. A 38 years old female with a history of deep venous thrombosis of the lower limb, presented with headache, vomiting and a generalized seizure. Magnetic resonance angiography showed a partial thrombosis of the left lateral and superior longitudinal venous sinuses. Coagulation study showed a resistance to activated C protein and factor V Leyden. A 42 years old woman with a history of deep venous thrombosis, presented a right hemiplegia during a hospitalization. Magnetic resonance showed a left lateral hemorrhagic infarction. Magnetic resonance angiography showed an absence of signal in three venous sinuses. Coagulation study showed a protein C deficiency. A 17 years old woman presented a right hemiparesis in the sixth day of puerperium. CAT scan showed a left frontoparietal subcortical venous infarction. Coagulation study showed an antithrombin III deficiency


Assuntos
Humanos , Feminino , Adulto , Adolescente , Trombofilia , Trombose Intracraniana , Tromboflebite , Fator V , Deficiência de Antitrombina III , Acenocumarol , Deficiência de Proteína C/fisiopatologia
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