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Updated: May 25, 2026

Transthoracic Echocardiography in Mice
Published on: May 28, 2010
Double-chambered left ventricle in echocardiography
Xiao-Yong Zhang1, Tie-Sheng Cao, Li-Jun Yuan
1Department of Ultrasound Diagnostics, Fourth Military Medical University, Xi'an, China.
Insights
A rare double-chambered left ventricle (LV) was identified in a 37-year-old man. Echocardiography proved valuable in diagnosing this anomaly, confirmed by advanced imaging techniques.
Area of Science:
- Cardiology
- Medical Imaging
- Anatomical Variations
Background:
- Congenital heart anomalies can present with diverse anatomical variations.
- A double-chambered left ventricle (LV) is an exceptionally rare congenital cardiac malformation.
Observation:
- A 37-year-old male presented with an unusual anatomical variation of the left ventricle.
- An accessory chamber was observed, attached to the inferior and posterior walls of the LV.
- This accessory chamber exhibited normal systolic function without regional wall motion abnormalities.
Findings:
- Echocardiography initially suggested the presence of a double-chambered LV.
- Cardiac computed tomography (CT) scanning and cardiac magnetic resonance (MR) imaging confirmed the diagnosis.
- The accessory chamber demonstrated preserved systolic contraction.
Implications:
- This case highlights the diagnostic utility of echocardiography in identifying rare cardiac anomalies.
- Advanced imaging modalities play a crucial role in confirming complex structural heart variations.
- Understanding such rare conditions improves diagnostic accuracy and patient management.
Abstract:
In this article, we describe a double-chambered left ventricle (LV) in a 37-year-old man. Its accessory chamber attached to the inferior and posterior wall of LV, and had normal systolic contraction without any regional wall motion abnormality. A double-chambered LV was suspected on echocardiography and confirmed by cardiac computed tomography scanning and cardiac magnet resonance imaging. Our aim is to accentuate the value of echocardiography in this rare anomaly
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