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Horseshoe lung associated with scimitar syndrome
Korcan Aysun Gonen1, Yakup Canitez2, Ozlem Mehtap Bostan2
1Department of Radiology, Namik Kemal University, Tekirdag, Turkey.
BMJ Case Reports
|August 18, 2019
Summary
Horseshoe lung, a rare congenital anomaly, involves fused lung bases and often includes scimitar syndrome. Multidetector CT (MDCT) effectively visualizes this complex condition in infants.
Area of Science:
- Medical Imaging
- Pediatric Radiology
- Congenital Anomalies
Background:
- Horseshoe lung is a rare congenital anomaly characterized by the fusion of the posterobasal segments of both lungs.
- It is frequently associated with scimitar syndrome, a condition involving abnormal venous return.
- Early and accurate diagnosis is crucial for managing associated cardiopulmonary complications.
Observation:
- This report details two cases of horseshoe lung in infant girls.
- Both presented with right lung hypoplasia and scimitar vein, an anomalous pulmonary vein draining into the inferior vena cava.
- Associated findings included dextroposition, atrial septal defects, pulmonary stenosis, and pulmonary hypertension.
Findings:
- Chest roentgenograms revealed dextroposition and mediastinal shift.
- Echocardiography identified secundum atrial septal defects and varying degrees of pulmonary hypertension and stenosis.
- Thoracic multidetector CT (MDCT) precisely delineated the fused lung isthmus, hypoplastic right lung and pulmonary artery, and the scimitar vein.
Implications:
- Multidetector CT (MDCT) is the gold standard for demonstrating the complex anatomy of horseshoe lung and associated anomalies.
- Understanding these imaging findings is vital for pediatricians and radiologists in diagnosing and planning treatment for affected infants.
- This case series highlights the spectrum of cardiovascular abnormalities that can accompany horseshoe lung and scimitar syndrome.
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