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Síndrome de Budd-Chiari e Trombocitopenia grave em doente com Lúpus Eritematoso Sistémico e Síndrome Antifosfolípido Secundária

dc.contributor.authorDuarte, C
dc.contributor.authorCouto, M
dc.contributor.authorInês, L
dc.contributor.authorMalcata, AB
dc.date.accessioned2008-12-11T16:28:52Z
dc.date.available2008-12-11T16:28:52Z
dc.date.issued2007
dc.description.abstractSystemic Lupus Erythematosus (SLE) is a rheumatic autoimmune disease characterized by multisystemic involvement with a variable prognosis. The association with Antiphospholipid Syndrome (APS) occurs in about 36% of the patients, raising additional problems with treatment and monitoring of these patients. The authors report a clinical case of a girl with SLE and APS who represented Budd-Chiari Syndrome and severe thrombocytopenia. The patient had severe thrombotic event and simultaneously a high hemorrhagic risk due to thrombocytopenia. Long-term resolution of the thrombocytopenia was achieved with mycophenolate mofetil. Long-term anticoagulation for thrombosis prophylaxis is requireden
dc.identifier.citationActa Reumatol Port. 2007 Apr-Jun;32(2):175-80en
dc.identifier.urihttp://hdl.handle.net/10400.4/327
dc.language.isoporen
dc.publisherSociedade Portuguesa de Reumatologiaen
dc.subjectLúpus Eritematoso Sistémicoen
dc.subjectSíndrome Antifosfolipídicoen
dc.subjectSíndrome de Budd-Chiarien
dc.subjectTrombocitopeniaen
dc.titleSíndrome de Budd-Chiari e Trombocitopenia grave em doente com Lúpus Eritematoso Sistémico e Síndrome Antifosfolípido Secundáriaen
dc.title.alternativeBudd-Chiari syndrome and severe thrombocytopenia in a patient with Systemic Lupus Erythematosus and Secondary Antiphospholipid Syndromeen
dc.typejournal article
dspace.entity.typePublication
rcaap.rightsopenAccess
rcaap.typearticleen

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