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A very rare case of late diagnosis of cor triatriatum sinistrum
Ingrid Schusterova1, Martin Czerny2, Alexander Jurko3
1Cardiac Surgery Clinic, Eastern Heart Institute, Kosice 04011, Slovakia.
Insights
A rare heart condition, cor triatriatum sinistrum, was found in a patient with a bicuspid aortic valve. Conservative treatment improved the patient's heart failure and atrial fibrillation symptoms.
Area of Science:
- Cardiology
- Congenital Heart Disease
Background:
- Cor triatriatum sinistrum is a rare congenital heart anomaly.
- Bicuspid aortic valve is a common congenital heart defect.
Observation:
- A 73-year-old patient with a history of heart failure, hypertension, and atrial fibrillation presented with these conditions.
- The patient was diagnosed with both cor triatriatum sinistrum and a bicuspid aortic valve.
Findings:
- The patient refused surgical correction for the diagnosed cardiac conditions.
- Conservative management of heart failure and atrial fibrillation led to symptomatic improvement.
Implications:
- This case highlights the importance of considering rare congenital anomalies in complex cardiac presentations.
- Conservative management can be effective for certain complex cardiac conditions, even in the absence of surgical intervention.
Abstract:
We presented a 73-year-old patient with a history of hospitalizations for heart failure as well as treatment for arterial hypertension and permanent atrial fibrillation and who was found to have cor triatriatum sinistrum in combination with bicuspid aortic valve. Patient refused surgical correction, but his condition improved on conservative therapy for heart failure and atrial fibrillation.
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