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Updated: Feb 14, 2026

Murine Echocardiography of Left Atrium, Aorta, and Pulmonary Artery
Published on: February 20, 2017
Congenital aneurysm of both left ventricle and left atrium
Ryan F Halas1, Christopher J Schmehil2, Gary R Ten Eyck3
1Department of Internal Medicine-Pediatrics, Western Michigan University Homer Stryker M.D. School of Medicine, Kalamazoo, MI, USA.
Insights
This case report details a rare instance of congenital left ventricular submitral aneurysm and left atrial appendage aneurysm in the same patient. The study highlights potential in utero causes and long-term clinical follow-up of these uncommon cardiac anomalies.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Cardiac Imaging
Background:
- Congenital left ventricular (LV) free wall submitral aneurysm and left atrial appendage aneurysm are individually rare cardiac malformations.
- Simultaneous occurrence of both lesions in a single patient is unprecedented in medical literature, suggesting a potential common etiology.
Observation:
- The case involved a fetus diagnosed with irregular heart rate and abnormal echocardiogram in the third trimester.
- The patient underwent emergent atrial appendage plication due to clot formation and experienced complications like ventricular ectopy and pseudoaneurysm.
- Long-term echocardiograms confirmed persistent LV aneurysm and maintained good LV function.
Findings:
- This is the first reported case of co-occurring congenital LV submitral aneurysm and left atrial appendage aneurysm.
- Potential in utero etiological factors, including maternal infections and antibiotic exposure, were considered.
- The clinical course involved significant complications necessitating surgical intervention and ongoing monitoring.
Implications:
- This case expands the understanding of rare cardiac anomalies and their potential co-occurrence.
- It underscores the importance of comprehensive fetal cardiac evaluation and long-term follow-up for congenital heart conditions.
- Further research into the etiology of these combined lesions may reveal shared developmental pathways or genetic predispositions.
Abstract:
This is a case of both congenital left ventricular (LV) free wall submitral aneurysm and left atrial appendage aneurysm with 6 years of clinical follow-up. Each lesion is a rare entity, and to the best of our knowledge, this is the first case in medical literature of both lesions occurring in the same patient, raising the likelihood of a common etiology. The workup was initiated in the third trimester of fetal life with irregular heart rate and abnormal fetal ultrasound and echocardiogram at that time. The patient required emergent atrial appendage plication due to blood clot formation and suffered from multiple other complications including ventricular ectopy and surgically induced pseudoaneurysm. Follow-up interval echocardiograms have revealed continued good LV function with persistent LV aneurysm. In review of the case, there were several potential in utero causes including maternal viral upper respiratory infection and bacteriuria with exposure to amoxicillin. These as well as other considerations are discussed along with a brief review of these rare lesions, usual presentation, and known associations.
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