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Updated: Jul 20, 2026

The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
A case report of atrial fibrillation in early adulthood: dig deeper
Abigail Masding1, Andreas Hoschtitzky1, Michael Gatzoulis1
1Royal Brompton Hospital, Sydney St, London SW3 6NP, UK.
Insights
A young adult with new-onset atrial fibrillation (AF) was diagnosed with cor triatriatum sinister (CTS), a rare congenital heart defect. Surgical correction restored sinus rhythm, improving quality of life.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Cardiac Arrhythmias
Background:
- Atrial fibrillation (AF) is a common arrhythmia often linked to underlying conditions.
- Congenital heart defects like atrial septal defects (ASDs) can predispose individuals to arrhythmias.
- Cor triatriatum sinister (CTS) is a rare congenital anomaly that can manifest later in life.
Observation:
- A 31-year-old man presented with new-onset AF, initially attributed to a viral illness.
- Recurrent AF and exercise intolerance led to further investigation.
- Transthoracic echocardiography revealed CTS, an ASD, and a patent foramen ovale.
Findings:
- Surgical intervention included membrane resection for CTS, Cox-maze procedure, and ASD closure.
- Sinus rhythm was successfully restored post-surgery.
- The patient experienced a return to baseline function and improved quality of life.
Implications:
- Young patients with new-onset AF require comprehensive cardiovascular evaluation to identify rare congenital causes.
- Early diagnosis and surgical management of CTS can effectively treat associated AF.
- Addressing congenital cardiac defects can significantly improve patient outcomes and quality of life.
Background:
Atrial fibrillation (AF) is a common cardiac arrhythmia, which is often associated with underlying risk factors and undiagnosed conditions, including congenital heart disease. Atrial septal defects (ASDs) come to mind, albeit arrhythmias usually present later in life. We present herewith a young patient with cor triatriatum sinister (CTS), with some delay in establishing the diagnosis, following new onset AF in early adulthood.
Case Summary:
A 31-year-old man presented with pre-syncope and coryzal symptoms and was newly diagnosed with AF in the context of an intercurrent viral illness. After treatment with oral anticoagulation and successful outpatient cardioversion, he was discharged from cardiology review. Two years later he re-presented with exercise intolerance and a 12-lead electrocardiogram revealing recurrence of AF. Subsequent investigation with transthoracic echocardiography revealed the underlying congenital cardiac defect of CTS, together with an ASD and patent foramen ovale. After corrective surgery, which involved membrane resection, a Cox-maze procedure and ASD closure, sinus rhythm was restored and at follow-up the patient had returned to baseline function.
Discussion:
Young patients presenting with new onset AF should undergo thorough cardiovascular assessment to identify treatable causes and reversible risk factors. Cor triatriatum sinister is a rare congenital anomaly that may present in adulthood and give rise to symptomatic AF. Surgical correction including a Cox-maze procedure in our patient resulted in restoration of sinus rhythm and a return of the patient's baseline functional status and improved quality of life.
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