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Updated: Feb 25, 2026

Echocardiographic Evaluation of Atrial Communications before Transcatheter Closure
Published on: February 8, 2022
Cor triatriatum and stroke
Jose Danilo Bengzon Diestro1, Joseph Justin Hipolito Regaldo2, Eddieson Masangcay Gonzales2
1Department of Neurosciences, Philippine General Hospital, University of the Philippines, Manila, Philippines.
Cor triatriatum sinistrum (CTS) is a rare congenital heart defect causing stroke. This case highlights treatment failures with antiplatelet and anticoagulant therapies in a young patient.
Area of Science:
- Cardiology
- Neurology
- Congenital Heart Disease
Background:
- Cor triatriatum sinistrum (CTS) is a rare congenital cardiac anomaly characterized by a fibromuscular membrane dividing the left atrium.
- CTS can lead to significant neurological complications, including stroke.
Observation:
- A 19-year-old female presented with a right middle cerebral artery (MCA) territory infarct.
- Diagnosis of CTS was confirmed via transthoracic echocardiography (TTE) showing a dividing membrane.
- The patient experienced recurrent strokes despite aspirin and later apixaban therapy.
Findings:
- This case represents the longest follow-up of a patient with CTS and stroke.
- It is the first reported instance of failure of both antiplatelet and anticoagulant therapies in managing CTS-related neurological events.
- The patient ultimately succumbed to hospital-acquired pneumonia following a third stroke.
Implications:
- This case underscores the potential for severe neurological morbidity in CTS.
- It challenges current treatment paradigms, suggesting limitations of standard antiplatelet and anticoagulant strategies in select CTS patients.
- Further research into optimal management of CTS to prevent thromboembolic events is warranted.
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