[Biventricular endomyocardiofibrosis associated with renal amyloidosis].

Arq Bras Cardiol

Universidade São Francisco, Bragança Paulista, Rua Benjamin Arruda 126/1, CEP 12914-560 Bragança Paulista, SP.

Published: October 2005

AI Article Synopsis

  • Endomyocardiofibrosis is a type of restrictive cardiomyopathy marked by fibrous tissue affecting the heart's inner lining and nearby muscle, leading to poor ventricular filling while keeping the heart's pumping ability intact.
  • Symptoms typically resemble heart failure, emphasizing the need for careful clinical examination to correctly identify the underlying cause.
  • The text presents a case of a patient who has biventricular endomyocardial fibrosis linked with renal amyloidosis, illustrating the complexity of diagnosing these conditions.

Article Abstract

Endomyocardiofibrosis is a restrictive cardiomyopathy characterized by fibrotic involvement of the endocardium and adjacent myocardium, and by diastolic dysfunction caused by changes in distensibility making ventricular filling inadequate while preserving the systolic function. Clinically, it appears as heart failure, but etiological symptomatic discernment, suspicion and a clinical examination would be necessary in order to make a correct etiological diagnosis. The case of a patient with biventricular endomyocardial fibrosis associated with renal amyloidosis is presented.

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http://dx.doi.org/10.1590/s0066-782x2005001700008DOI Listing

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