Asymptomatic discovery of a rare congenital vascular anomaly in a 33-year-old male: a case of Pulmonary Sling Syndrome
Bayram Altuntaş1,Hacer Bal2
Current Thoracic Surgery
2026;11(1):105-108.
1Department of Thoracic Surgery, Life Hospital, Antalya, Türkiye
2Department of Radiology, Life Hospital, Antalya, Türkiye
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Pulmonary sling (PS) syndrome is a rare congenital vascular anomaly characterized by the anomalous
origin of the left pulmonary artery (LPA) from the right pulmonary artery (RPA). While it typically
presents in infancy with severe respiratory distress, its diagnosis in adulthood is exceedingly rare and
often incidental. A 33-year-old male presented with acute, severe right-sided pleuritic chest pain.
Initial suspicion was pulmonary embolism (PE); however, laboratory markers (D-dimer, troponin) were
normal. Pulmonary CT angiography ruled out PE but revealed an incidental pulmonary sling, where the
LPA originated from the RPA and coursed between the trachea and esophagus. A 10 mm pleural effusion
was noted. The patient was diagnosed with idiopathic pleurisy, treated with anti-inflammatory agents,
and symptoms resolved. This case underscores the possibility of PS remaining asymptomatic until the
fourth decade of life. Clinicians should be aware of such vascular variants, as they may have significant
implications for airway management and thoracic surgery.
Keywords :
pulmonary artery, vascular ring, incidental findings