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Loeffler endocarditis: silent right ventricular myocardium!

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dc.contributor.authors Cetin, S; Heper, G; Vural, MG; Hazirolan, T;
dc.date.accessioned 2020-02-27T07:19:46Z
dc.date.available 2020-02-27T07:19:46Z
dc.date.issued 2016
dc.identifier.citation Cetin, S; Heper, G; Vural, MG; Hazirolan, T; (2016). Loeffler endocarditis: silent right ventricular myocardium!. WIENER KLINISCHE WOCHENSCHRIFT, 128, 515-513
dc.identifier.issn 0043-5325
dc.identifier.uri https://doi.org/10.1007/s00508-016-0981-1
dc.identifier.uri https://hdl.handle.net/20.500.12619/65460
dc.description.abstract We present the case of a 54-year-old male patient with Loeffler endocarditis. It is a rare disorder characterized by fibrous thickening of the endocardium leading to apical obliteration and restrictive cardiomyopathy resulting in heart failure, thromboembolic events or atrial fibrillation. To the best of our knowledge, this is the first case reporting the electrical silence of the right ventricular (RV) apex caused by fibrothrombotic thickening of this area. Under these circumstances RV apical implantation of an implantable cardioverter defibrillator (ICD) or pacemaker electrode may lead to unsuccessful stimulation of these devices.
dc.language English
dc.publisher SPRINGER WIEN
dc.subject General & Internal Medicine
dc.title Loeffler endocarditis: silent right ventricular myocardium!
dc.type Article
dc.identifier.volume 128
dc.identifier.startpage 513
dc.identifier.endpage 515
dc.contributor.department Sakarya Üniversitesi/Tıp Fakültesi/Temel Tıp Bilimleri Bölümü
dc.contributor.saüauthor Vural, Mustafa Gökhan
dc.relation.journal WIENER KLINISCHE WOCHENSCHRIFT
dc.identifier.wos WOS:000380123500006
dc.identifier.doi 10.1007/s00508-016-0981-1
dc.identifier.eissn 1613-7671
dc.contributor.author Suha Cetin
dc.contributor.author Gulumser Heper
dc.contributor.author Vural, Mustafa Gökhan
dc.contributor.author Tuncay Hazirolan


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