dc.creatorPivatto Júnior, Fernando
dc.creatorPiardi, Diogo Silva
dc.creatorTorres, Felipe Soares
dc.date2015-01-16
dc.identifierhttps://seer.ufrgs.br/index.php/hcpa/article/view/51436
dc.descriptionErdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis of unknown etiology characterized by proliferation of lipid-containing foamy histiocytes affecting bones and potentially every organ. There is a wide clinical spectrum of the disease, ranging from asymptomatic bone or soft-tissue lesions to life-threatening systemic involvement. Although the initial descriptions published by Jakob Erdheim and William Chester in 1930 included a patient with right atrial infiltration on autopsy, cardiovascular involvement in ECD has only gained more recognition recently. In the present report, we describe a case with cardiac involvement, presenting with symptomatic heart failure and a cardiac mass assessed with echocardiogram and cardiac magnetic resonance imaging.en-US
dc.formatapplication/pdf
dc.languageeng
dc.publisherHCPA/FAMED/UFRGSpt-BR
dc.relationhttps://seer.ufrgs.br/index.php/hcpa/article/view/51436/33155
dc.sourceClinical & Biomedical Research; Vol. 34 No. 4 (2014)en-US
dc.sourceClinical and Biomedical Research; v. 34 n. 4 (2014)pt-BR
dc.source2357-9730
dc.subjectErdheim-Chester diseaseen-US
dc.subjectheart failureen-US
dc.subjectmagnetic resonance imagingen-US
dc.titleCardiac involvement in Erdheim-Chester disease: a case report.en-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typePeer-reviewed Articleen-US
dc.typeAvaliado por parespt-BR


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