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Cor triatriatum: unusual cause of transient ischaemic attacks in a 67-year-old man

D Darbar1, A B Bridges, R Roberts

  • 1Department of Cardiology, Ninewells Hospital and Medical School, Dundee, Scotland.

The British Journal of Clinical Practice
|May 1, 1995
PubMed

Insights

This study presents a rare congenital heart defect, cor triatriatum, diagnosed late in a 67-year-old patient presenting with neurological symptoms. Echocardiography proved vital in diagnosing this condition and identifying potential embolic sources.

Area of Science:

  • Cardiology
  • Neurology
  • Congenital Heart Disease

Background:

  • Cor triatriatum is a rare congenital cardiac malformation.
  • Characterized by a membrane dividing the left atrium into two chambers.
  • Late adult presentation is uncommon, with this case being one of the oldest at 67 years.

Observation:

  • Patient presented with symptoms suggestive of embolic events: transient ischemic attack (TIA), episodic vertigo, and central retinal artery occlusion.
  • Diagnosis of cor triatriatum was established following these neurological events.

Findings:

  • Echocardiography confirmed the presence of cor triatriatum.
  • The imaging modality was crucial in evaluating the cardiac source of potential emboli.

Implications:

  • Highlights the importance of considering congenital cardiac anomalies in adult-onset neurological deficits.
  • Demonstrates the diagnostic utility of echocardiography in cases of presumed embolic neurological disease.
  • Underscores that cor triatriatum can manifest symptomatically even in advanced age.

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