Pediatric scimitar syndrome with an intrahepatic venous-venous shunt: A rare imaging case report

Scimitar syndrome (pulmonary veno-lobular syndrome) is a rare congenital anomaly characterized by abnormal pulmonary venous drainage. The coexistence of this syndrome with a veno-venous shunt connecting an accessory hepatic vein to the main hepatic vein is exceptionally rare; to our knowledge, this is the first such case reported in an asymptomatic patient. A pediatric patient was referred to cardiology following the incidental discovery of a heart murmur during a routine exam. While the patient was asymptomatic, an echocardiogram revealed mitral valve regurgitation and right-sided heart dilation. A chest X-ray showed the classic “scimitar” sign (a curved paracardiac opacity). Subsequent CT angiography confirmed that the entire right lung drained into the inferior vena cava and identified an incidental veno-venous shunt between the inferior right accessory hepatic vein and the main hepatic vein. This report highlights a unique variant of Scimitar syndrome involving an unusual hepatic vascular shunt. It underscores the critical role of advanced imaging in detecting latent vascular anomalies, even when clinical symptoms are absent.

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Publication Details

Journal
Radiology Case Reports
Published
2026-07-30
DOI
https://doi.org/10.1016/j.radcr.2026.06.077
Primary Topic
Congenital Diaphragmatic Hernia Studies
Type
article
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article

Pediatric scimitar syndrome with an intrahepatic venous-venous shunt: A rare imaging case report

Ermela Çelaj, Marjeta Tanka, Numila Kuneshka, Erjona Abazaj et al.
Radiology Case Reports
Congenital Diaphragmatic Hernia Studies
article

Pediatric scimitar syndrome with an intrahepatic venous-venous shunt: A rare imaging case report

Ermela Çelaj, Marjeta Tanka, Numila Kuneshka, Erjona Abazaj, Albert Koja, Fjorda Tuka, Vasiana Tanka, Kostandin Tanka
article en

Abstract

Scimitar syndrome (pulmonary veno-lobular syndrome) is a rare congenital anomaly characterized by abnormal pulmonary venous drainage. The coexistence of this syndrome with a veno-venous shunt connecting an accessory hepatic vein to the main hepatic vein is exceptionally rare; to our knowledge, this is the first such case reported in an asymptomatic patient. A pediatric patient was referred to cardiology following the incidental discovery of a heart murmur during a routine exam. While the patient was asymptomatic, an echocardiogram revealed mitral valve regurgitation and right-sided heart dilation. A chest X-ray showed the classic “scimitar” sign (a curved paracardiac opacity). Subsequent CT angiography confirmed that the entire right lung drained into the inferior vena cava and identified an incidental veno-venous shunt between the inferior right accessory hepatic vein and the main hepatic vein. This report highlights a unique variant of Scimitar syndrome involving an unusual hepatic vascular shunt. It underscores the critical role of advanced imaging in detecting latent vascular anomalies, even when clinical symptoms are absent.

Radiology Case ReportsVol. 21(10)
University of Medicine Tirana (AL), Mother Teresa Hospital (AL), Medical University of Vienna (AT)
Openalex Percentile: Top 7%
Congenital Diaphragmatic Hernia Studies
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