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Three-Dimensional Echocardiographic Method for the Visualization and Assessment of Specific Parameters of the Pulmonary Veins
Published on: October 28, 2020
Isolated and complex scimitar vein anomalies and their differentiation from the meandering right pulmonary vein
1Department of Pediatrics, Division of Pediatric Cardiology, Changhua Christian Hospital, No. 135, Nanhsiao St., Changhua 50050, Taiwan. ferdielee@yahoo.com
Insights
Scimitar vein anomalies in children present with varied symptoms, including infections and heart failure. Differentiating types of scimitar vein anomaly is vital for patient outcomes.
Area of Science:
- Pediatric Cardiology
- Thoracic Surgery
- Medical Imaging
Background:
- Scimitar vein anomaly is a rare congenital condition affecting pulmonary venous return.
- It can occur in isolated or complex forms, with varying associated malformations.
Purpose of the Study:
- To review and compare pediatric patients with isolated and complex scimitar vein anomalies.
- To analyze clinical presentations and diagnostic findings in these patients.
Main Methods:
- Retrospective study of 4 female pediatric patients (2 days to 3.5 years) with scimitar vein anomalies.
- Review of clinical features, imaging (radiography, echocardiography, MRI, MRA, CT), bronchography, cardiac catheterization, surgery, and autopsy records.
Main Results:
- Clinical manifestations included lung infections, respiratory distress, heart failure, pulmonary hypertension, cyanosis, dextrocardia, heterotaxy, and right atrial isomerism.
- Two patients with right atrial isomerism expired, highlighting the severity of complex cases.
Conclusions:
- Clinical differentiation between scimitar vein anomaly with and without cardiovascular and bronchopulmonary malformations is critical.
- Accurate diagnosis and classification are essential for predicting patient outcomes.
Purpose:
Four pediatric patients with isolated (the adult form) and complex (the infantile form) scimitar vein anomalies were reviewed and compared with patients with meandering right pulmonary veins.
Materials And Methods:
From January 1990 to December 2006, 4 female patients, aged 2 days to 3.5 years, with isolated and complex scimitar vein anomalies were retrospectively studied. The clinical features, chest radiographs, echocardiography, magnetic resonance imaging, magnetic resonance angiography, computer tomography, bronchography, cardiac catheterization with angiography, surgery, and autopsy were reviewed to substantiate the diagnosis of isolated and complex scimitar vein anomalies.
Results:
Clinical manifestations were lung infections with radiographic scimitar signs in 4 patients (3 right; 1 left), respiratory distress, congestive heart failure, pulmonary hypertension and/or cyanosis in 3 patients, dextrocardia, heterotaxy, and/or right atrial isomerism in 2 patients, as well as dextroversion, right bronchial isomerism, bronchial stenosis, and/or sepsis in 1 patient. Two patients with right atrial isomerism expired.
Conclusion:
The clinical discrimination between scimitar vein anomaly with and without cardiovascular and bronchopulmonary malformations is crucial for the outcomes vary.
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