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Hepatogastroenterology ; 50(50): 512-4, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-12749260

RESUMEN

Here we describe two women with polycythemia vera presented with fulminant hepatic failure due to acute Budd-Chiari syndrome. Both had a history of severe abdominal pain and distention of short duration. Clinical and laboratory findings showed fulminant hepatic failure due to acute Budd-Chiari syndrome. Diagnosis was confirmed with abdominal ultrasonography and Doppler ultrasonography showing ascites, hepatomegaly, portal hypertension and total occlusion of hepatic veins. Complete blood count and other clinical findings were compatible with polycythemia vera in both patients. Patients were treated successfully with early administration of continuous heparin infusion, repeated phlebotomies and hydroxyurea. We emphasize here early diagnosis and effective treatment in such fulminant cases may be life saving.


Asunto(s)
Anticoagulantes/uso terapéutico , Síndrome de Budd-Chiari/tratamiento farmacológico , Síndrome de Budd-Chiari/etiología , Heparina/uso terapéutico , Hidroxiurea/uso terapéutico , Policitemia Vera/complicaciones , Enfermedad Aguda , Adulto , Síndrome de Budd-Chiari/diagnóstico , Quimioterapia Combinada , Femenino , Humanos , Fallo Hepático/etiología
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