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Cardiac Angiosarcoma. A Review

dc.contributor.authorMurinello, A
dc.contributor.authorMendonça, P
dc.contributor.authorAbreu, A
dc.contributor.authorSantos, AL
dc.contributor.authorRoquette, J
dc.contributor.authorPinto, E
dc.contributor.authorAlpendra, J
dc.contributor.authorSemedo, J
dc.contributor.authorRodrigues, A
dc.contributor.authorCunha, D
dc.contributor.authorCoelho, JF
dc.contributor.authorLourenço, S
dc.contributor.authorMiranda, S
dc.date.accessioned2012-08-17T15:23:56Z
dc.date.available2012-08-17T15:23:56Z
dc.date.issued2007
dc.description.abstractBased on a case of a patient with angiosarcoma (AS) of the right atrium with superior vena cava syndrome associated with urticaria and polyarthralgias, who died soon after surgery, the authors present a brief review of the subject of cardiac AS, an extremely rare pathology, usually diagnosed late due to its non-specific symptomatology. Several topics are discussed, including mechanisms of clinical manifestations caused by blood flow obstruction and valve dysfunction, local invasion with arrhythmias and pericardial effusion, embolic phenomena and constitutional symptoms. Imaging and histopathologic methods of diagnosis are considered, as well as references to cytogenetic analysis. Surgery is the first treatment choice, but heart AS are frequently not completely resectable and concomitant metastases at the time of surgery are common, both usually leading to a dismal prognosis. Chemotherapy, radiotherapy and even heart transplantation do not substantially improve the survival of these patients. Urticaria is not generally assumed by most authors to be associated with malignancy, but there are rare reports of its association with some malignant tumors.por
dc.identifier.citationRev Port Cardiol. 2007 May;26(5):577-84por
dc.identifier.urihttp://hdl.handle.net/10400.17/623
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherSociedade Portuguesa de Cardiologiapor
dc.subjectNeoplasias Cardíacaspor
dc.subjectAngiosarcomapor
dc.subjectHCC MED
dc.subjectHCC DER
dc.subjectHSM CAR
dc.subjectHSM CCT
dc.subjectHSM ANPAT
dc.titleCardiac Angiosarcoma. A Reviewpor
dc.title.alternativeAngiosarcoma Cardíaco. Uma Revisãopor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage584por
oaire.citation.startPage577por
oaire.citation.titleRevista Portuguesa de Cardiologiapor
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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