| Literature DB >> 27144839 |
Cintia Prado Maia1, Luís Gustavo Gali1, André Schmidt1, Oswaldo César de Almeida Filho1, Marcel Koenigkam Santos2, Luciano Albuquerque Lima Saraiva1, Alfredo José Rodrigues3, Benedito Carlos Maciel1, Minna Moreira Dias Romano1.
Abstract
Endomyocardial fibrosis, which is a cause of restrictive cardiomyopathy, is characterized by the deposition of fibrous tissue in the apical region of 1 or both ventricles. The condition not only affects the diastolic dynamics of the ventricles, but also the function of the atrioventricular valves. The disease occurs predominantly in tropical regions worldwide and in sub-Saharan Africa. This condition is not well understood, with varied manifestations, from subclinical presentations to chronic and progressive edematous syndromes. Here, we present the challenging case of a patient with an indeterminate echocardiographic image, suggesting apical hypertrophy, plus severe aortic stenosis and fibrosis of the left ventricular outflow tract. An electrocardiogram revealed symmetrical T-wave inversion, which is a characteristic manifestation of apical hypertrophy. The importance of cardiac imaging examinations such as echocardiography and cardiac magnetic resonance for differentiating between endomyocardial fibrosis and apical hypertrophy is highlighted in this patient's case.Entities:
Keywords: cardiac magnetic resonance; echocardiography; endomyocardial fibrosis; restrictive cardiomyopathy
Mesh:
Year: 2016 PMID: 27144839 DOI: 10.1111/echo.13244
Source DB: PubMed Journal: Echocardiography ISSN: 0742-2822 Impact factor: 1.724