Rare diagnosis of Ebstein anomaly in an adult patient in Northern Rio de Janeiro

Authors

  • Rogerio Muylaert de Carvalho Britto Faculdade de Medicina de Campos
  • Adail Orrith Liborio Neto Universidade Federal do Rio de Janeiro Campus Macaé http://orcid.org/0000-0002-1674-4317
  • Otávio Defanti Ramos Faculdade de Medicina de Campos
  • Mirele da Silva Cruz Defanti Faculdade de Medicina de Campos

Keywords:

Ebstein anomaly, Adult, Insufficiency of the tricuspid valve, Echocardiography

Abstract

Ebstein anomaly is the fourth most frequent cyanotic heart disease in the neonatal period, and its clinical course is slow compared to other diseases, which in turn results in late diagnosis of this condition. We present a case of a 37-year-old man who complained of palpitation for about 5 years, twice a week, at rest, with prolonged duration and low systemic output. Auscultation revealed irregular heart rhythm characterized by extrasystoles with a tricuspid systolic murmur grade 5+/6 and worsening on inspiration. Clinical spectrum is variable and depends on the severity of defects and associated anatomical changes. In patients who have reached adulthood, symptoms usually present as progressive cyanosis, exercise intolerance, right heart failure, and arrhythmias. In Brazil, identification of this congenital disease usually occurs in a more adult phase, affecting the prognosis and survival of patients.

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Author Biography

Mirele da Silva Cruz Defanti, Faculdade de Medicina de Campos

Médica Cardiologista.

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Published

2021-07-26

How to Cite

1.
Britto RM de C, Liborio Neto AO, Ramos OD, Defanti M da SC. Rare diagnosis of Ebstein anomaly in an adult patient in Northern Rio de Janeiro. Clin Biomed Res [Internet]. 2021Jul.26 [cited 2022May21];41(2). Available from: https://www.seer.ufrgs.br/index.php/hcpa/article/view/101366

Issue

Section

Case Report