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Adults forms of scimitar syndrome
Reda Mounir1, Fouad Nya1, Belkhadir Mohammed1
1Department of Cardiac Surgery, Mohamed 5 Military Hospital, Faculty of Medecine and Pharmacy, Rabat, Morocco.
Journal of Cardiac Surgery
|May 24, 2020
Summary
Scimitar syndrome, a rare venous malformation, often goes undiagnosed in adults due to mild symptoms. This report details two adult cases, highlighting the importance of recognizing this condition in later life.
Area of Science:
- Cardiology
- Thoracic Surgery
- Medical Imaging
Background:
- Scimitar syndrome is a rare congenital heart defect characterized by anomalous pulmonary venous return from the right lung.
- The condition involves the right pulmonary veins draining into the inferior vena cava instead of the left atrium.
- Severe cases are typically diagnosed in infancy or childhood, while milder forms may remain asymptomatic in adults.
Observation:
- This report presents two adult cases of Scimitar syndrome.
- One patient presented with chest discomfort, a less common symptom in adults with this condition.
- The diagnosis in adults is often incidental or delayed due to the subtle presentation.
Findings:
- Adult-onset Scimitar syndrome can present with varied symptoms, including chest discomfort.
- Mild forms of anomalous pulmonary venous return may not manifest until adulthood.
- Diagnostic imaging, such as echocardiography and CT pulmonary angiography, is crucial for identification.
Implications:
- Increased awareness of Scimitar syndrome in adults is necessary for timely diagnosis and management.
- Early recognition can prevent potential complications associated with undiagnosed anomalous pulmonary venous return.
- Further research into the long-term outcomes and optimal treatment strategies for adult Scimitar syndrome is warranted.
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