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Dynamic three-dimensional echocardiography in the assessment of cor triatriatum

C Melzer1, T Bartel, S Müller

  • 1Medizinische Klinik I., Charité, Humboldt University, Berlin, Germany.

Clinical Cardiology
|January 1, 1997
PubMed

Insights

Cor triatriatum sinistrum, a rare heart defect, was diagnosed in an adult after atrial septal defect surgery. Dynamic 3-D echocardiography confirmed the accessory membrane was not stenosing, thus surgical correction was not needed.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Congenital Heart Disease

Background:

  • Cor triatriatum sinistrum is a rare congenital heart malformation.
  • It is infrequently diagnosed in adults, often presenting after other cardiac interventions.
  • This case highlights a delayed diagnosis in a 55-year-old male post-atrial septal defect repair.

Observation:

  • Transesophageal echocardiography (TEE) diagnosed cor triatriatum sinistrum one year after surgical correction of an atrial septal defect.
  • The study compared transthoracic echocardiography (TTE), TEE, and cardiac catheterization against dynamic three-dimensional echocardiography (3-D echo).
  • 3-D echo provided a novel, noninvasive method to assess the opening size between the accessory and true left atrium.

Findings:

  • Dynamic 3-D echo accurately determined the opening size of the accessory membrane.
  • Left heart catheterization confirmed the findings from 3-D echo.
  • The accessory membrane was found to be non-stenosing in this patient.

Implications:

  • Dynamic 3-D echocardiography is a valuable noninvasive tool for evaluating cor triatriatum sinistrum.
  • Accurate assessment of membrane stenosis can prevent unnecessary surgical interventions.
  • This case underscores the importance of considering rare cardiac malformations even after previous cardiac surgery.

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