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Arteria lusoria is a rare congenital vascular anomaly in which the right subclavian artery takes an abnormal course behind the esophagus, potentially causing swallowing difficulties.
Arteria lusoria is a rare congenital vascular anomaly in which the right subclavian artery takes an abnormal course behind the esophagus, potentially causing swallowing difficulties.
Arteria lusoria (Latin for "playful artery") is one of the most common congenital anomalies of the aortic arch. It occurs when the right subclavian artery does not arise in its usual position from the brachiocephalic trunk but instead originates directly from the aortic arch – typically as its last branch. The vessel then travels behind the esophagus (retroesophageal), or less commonly between the esophagus and the trachea. This vascular malformation affects approximately 0.5 to 2% of the population, making it the most frequently encountered aortic arch anomaly.
Arteria lusoria arises during embryonic development due to a malformation of the aortic arch arteries. During normal fetal development, paired pharyngeal arch arteries develop into the major vessels of the thorax. An abnormal regression of the fourth right aortic arch leads to the atypical origin and course of the right subclavian artery. The condition is generally considered to have a genetic basis, and an association with certain chromosomal disorders – such as trisomy 21 (Down syndrome) – has been reported.
The majority of individuals with arteria lusoria are completely asymptomatic, and the anomaly is often discovered incidentally during imaging for other reasons. When symptoms do occur, they typically result from mechanical compression of adjacent structures:
Symptoms can occur at any age but often first appear in adulthood, when degenerative changes such as atherosclerosis cause stiffening of the vessel, increasing pressure on the esophagus.
Arteria lusoria is frequently discovered as an incidental finding during imaging studies. The most important diagnostic methods include:
Asymptomatic arteria lusoria generally does not require treatment and is managed with periodic follow-up. For patients with significant symptoms, the following options are available:
In mild cases, dietary adjustments (such as soft food and slow eating) and treatment of contributing conditions (such as atherosclerosis) may help relieve discomfort.
In cases of severe or progressive symptoms, surgical intervention is indicated. Treatment options include:
The prognosis following surgical treatment is generally excellent, with most patients experiencing complete resolution of swallowing difficulties.
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