Medicine:Aberrant subclavian artery

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Aberrant subclavian artery
Other namesAberrant subclavian artery syndrome
Arteria lusoria MRA MIP-03 - Annotated.jpg

Aberrant subclavian artery, or aberrant subclavian artery syndrome, is a rare anatomical variant of the origin of the right or left subclavian artery. This abnormality is the most common congenital vascular anomaly of the aortic arch,[1] occurring in approximately 1% of individuals.[1][2][3]

Presentation

This condition is usually asymptomatic.[1] The aberrant artery usually arises just distal to the left subclavian artery and crosses in the posterior part of the mediastinum on its way to the right upper extremity.[2] In 80% of individuals it crosses behind the esophagus.[2] Such course of this aberrant vessel may cause a vascular ring around the trachea and esophagus. Dysphagia due to an aberrant right subclavian artery is termed dysphagia lusoria, although this is a rare complication.[2][3] In addition to dysphagia, aberrant right subclavian artery may cause stridor, dyspnoea, chest pain, or fever.[1] An aberrant right subclavian artery may compress the recurrent laryngeal nerve causing a palsy of that nerve, which is termed Ortner's syndrome.[4]

The aberrant right subclavian artery frequently arises from a dilated segment of the proximal descending aorta, the so-called Diverticulum of Kommerell (which was named for the German radiologist Burkhard Friedrich Kommerell (1901–1990), who discovered it in 1936).[5][6] It is alternatively known as a lusorian artery.[1][3]

Pathophysiology

The embryological basis of the retroesophageal aberrant right subclavian artery

In the normal embryological development of the aortic arches, the right dorsal aorta regresses caudal to the origin of the 7th intersegmental artery which gives rise to the right subclavian artery. In formation of an aberrant right subclavian artery, the regression occurs instead between the 7th intersegmental artery and the right common carotid so that the right subclavian artery is then connected to the left dorsal aorta via the part of the right dorsal aorta which normally regresses. During growth, the origin of the right subclavian artery migrates until it is just distal to that of the left subclavian.[3]

Diagnosis

Treatment

Surgery is occasionally used to treat the condition.[7]

Images

See also

  • Dysphagia lusoria

References

  1. 1.0 1.1 1.2 1.3 1.4 Mahmodlou, Rahim; Sepehrvand, Nariman; Hatami, Sanaz (2014). "Aberrant Right Subclavian Artery: A Life-threatening Anomaly that should be considered during Esophagectomy". Journal of Surgical Technique and Case Report 6 (2): 61–63. doi:10.4103/2006-8808.147262. PMID 25598945. 
  2. 2.0 2.1 2.2 2.3 Kau, Thomas; Sinzig, Marietta; Gasser, Johann; Lesnik, Gerald; Rabitsch, Egon; Celedin, Stefan; Eicher, Wolfgang; Illiasch, Herbert et al. (2007). "Aortic Development and Anomalies". Seminars in Interventional Radiology 24 (2): 141–152. doi:10.1055/s-2007-980040. PMID 21326792. 
  3. 3.0 3.1 3.2 3.3 Chaoui, R; Rake, A; Heling, KS (2008). "Aortic arch with four vessels: aberrant right subclavian artery". Ultrasound in Obstetrics and Gynecology 31 (1): 115–117. doi:10.1002/uog.5240. PMID 18098341. 
  4. Bickle, IC; Kelly, BE; Brooker, DS (2002). "Ortner's syndrome: a radiological diagnosis". The Ulster Medical Journal 71 (1): 55–56. PMID 12137166. 
  5. St-Amant, Maxime. "Kommerell diverticulum (right aberrant subclavian artery)". https://radiopaedia.org/cases/kommerell-diverticulum-right-aberrant-subclavian-artery. 
  6. Jha, Praveen. "Kommerell diverticulum". https://radiopaedia.org/articles/kommerell-diverticulum. 
  7. "Aberrant subclavian artery and Kommerell aneurysm: surgical treatment with a standard approach". The Journal of Thoracic and Cardiovascular Surgery 133 (4): 888–92. April 2007. doi:10.1016/j.jtcvs.2006.12.005. PMID 17382621. 

External links

Classification