dc.creator | Pivatto Júnior, Fernando | |
dc.creator | Piardi, Diogo Silva | |
dc.creator | Torres, Felipe Soares | |
dc.date | 2015-01-16 | |
dc.identifier | https://seer.ufrgs.br/index.php/hcpa/article/view/51436 | |
dc.description | Erdheim-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.format | application/pdf | |
dc.language | eng | |
dc.publisher | HCPA/FAMED/UFRGS | pt-BR |
dc.relation | https://seer.ufrgs.br/index.php/hcpa/article/view/51436/33155 | |
dc.source | Clinical & Biomedical Research; Vol. 34 No. 4 (2014) | en-US |
dc.source | Clinical and Biomedical Research; v. 34 n. 4 (2014) | pt-BR |
dc.source | 2357-9730 | |
dc.subject | Erdheim-Chester disease | en-US |
dc.subject | heart failure | en-US |
dc.subject | magnetic resonance imaging | en-US |
dc.title | Cardiac involvement in Erdheim-Chester disease: a case report. | en-US |
dc.type | info:eu-repo/semantics/article | |
dc.type | info:eu-repo/semantics/publishedVersion | |
dc.type | Peer-reviewed Article | en-US |
dc.type | Avaliado por pares | pt-BR |