Púrpura trombocitopénico trombótico con respuesta exitosa a vincristina

dc.contributor.authorFrancisco Espinoza
dc.contributor.authorJosé Luis Leal
dc.contributor.authorGuillermo Arenas
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T16:43:49Z
dc.date.available2026-03-22T16:43:49Z
dc.date.issued2007
dc.descriptionCitaciones: 1
dc.description.abstractThrombotic thrombocytopenic purpura presents as a multisystemic disease with thrombocytopenia, microangiopathic hemolytic anemia, fever, neurological and renal involvement. We report a 24 years-old male presenting with purpura and a generalized seizure. His blood tests showed an hemolytic anemia, unconjugated hyperbilirubinemia, increased lactated dehydrogenase, thrombocytopenia and impairment of renal function. He was initially treated with daily plasmapheresis and steroids without improvement. Due to persistence of the disease, he was treated with two doses of intravenous vincristine in four days, with clinical and laboratory improvement. He was discharged 40 days after the last dose of vincristine, in good conditions.
dc.identifier.doi10.4067/s0034-98872007001200011
dc.identifier.urihttps://doi.org/10.4067/s0034-98872007001200011
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/59965
dc.language.isoes
dc.publisherQ16635223
dc.relation.ispartofRevista médica de Chile
dc.sourceUniversidad de Los Andes
dc.subjectMedicine
dc.subjectMicroangiopathic hemolytic anemia
dc.subjectPlasmapheresis
dc.subjectThrombotic thrombocytopenic purpura
dc.subjectVincristine
dc.subjectHemolytic anemia
dc.subjectGastroenterology
dc.subjectInternal medicine
dc.subjectAnemia
dc.subjectSchistocyte
dc.titlePúrpura trombocitopénico trombótico con respuesta exitosa a vincristina
dc.typearticle

Files