DOI: 10.12890/2025_005044

Scimitar syndrome: unveiling the complexities of a rare congenital cardiopulmonary anomaly

Authors

  • Nargis Mateen Department of Internal Medicine, St. Josephs University Medical Center, Paterson, USA
  • Abraam Rezkalla Department of Internal Medicine, St. Josephs University Medical Center, Paterson, USA
  • Nagihan Orhun Department of Internal Medicine, St. Josephs University Medical Center, Paterson, USA

nargistmateen@gmail.com

Keywords

Scimitar syndrome, pulmonary hypoplasia, asthma exacerbation, dextrocardia, rare congenital anomaly

Abstract

Scimitar syndrome is a rare congenital anomaly characterised by anomalous pulmonary venous drainage of the right lung into the inferior vena cava, often accompanied by right lung hypoplasia and dextroposition of the heart. Here, we present the case of a 24-year-old female with scimitar syndrome and a history of asthma who presented with acute exacerbation of asthma. A chest X-ray revealed opacification of the right hemithorax, and a CT angiography revealed congenital hypoplasia of the right lung and dextrocardia. This report provides a detailed description of scimitar syndrome to spread awareness of this rare diagnosis and highlights the unique and various constellations of anatomical abnormalities seen in scimitar syndrome that make diagnosis difficult.

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References

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Published

2025-02-07

How to Cite

1.
Mateen N, Rezkalla A, Orhun N. Scimitar syndrome: unveiling the complexities of a rare congenital cardiopulmonary anomaly. EJCRIM [Internet]. 2025 Feb. 7 [cited 2026 Nov. 3];12(3). Available from: https://ejcrim.com/index.php/ejcrim/article/view/5044

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