Report of an atypical case with arrhythmogenic right ventricular dysplasia or Uhl´s anomaly

Authors

  • Luis M. Morales Pérez Instituto de Cardiología y Cirugía Cardiovascular
  • Omar R. González Greck Instituto de Cardiología y Cirugía Cardiovascular
  • Ana M. Jerez Castro Instituto de Cardiología y Cirugía Cardiovascular
  • Eliezer San Román García Instituto de Cardiología y Cirugía Cardiovascular
  • Aníbal González Trujillo Instituto de Cardiología y Cirugía Cardiovascular

Keywords:

arrhythmogenic right ventricular dysplasia, cardiomyopathy

Abstract

Arrhythmogenic right ventricular dysplasia is a cardiomyopathy characterized by malignant ventricular arrhythmias and progressive structural abnormalities, affecting primarily the right ventricle. It appears due to a partial or massive progressive replacement of the myocardium by fibroadipose or adipose tissue. Uhl's disease may be an extreme and widespread manifestation of arrhythmogenic right ventricular dysplasia, a rare congenital disorder with absence of right ventricular myocardium, so that its walls are paper thin. The case of a 56 year old male patient who had loss of consciousness and underwent clinical and echocardiographic diagnosis is presented. The clinical features, diagnosis and action to take against this potentially fatal heart disease in patients with syncope, ventricular tachycardia or cardiac arrest are discussed.

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References

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Published

2012-12-03

How to Cite

1.
Morales Pérez LM, González Greck OR, Jerez Castro AM, San Román García E, González Trujillo A. Report of an atypical case with arrhythmogenic right ventricular dysplasia or Uhl´s anomaly. CorSalud [Internet]. 2012 Dec. 3 [cited 2025 Oct. 2];4(4):300-6. Available from: https://revcorsalud.sld.cu/index.php/cors/article/view/1245

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CASE REPORTS

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