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Pathology · Cardiovascular Pathology

Coarctation of the aorta

Coarctatio aortae

Aortic coarctation is a congenital narrowing of the vessel at the junction of the aortic arch and the descending segment. This condition leads to severe hemodynamic disturbances, including upper-extremity hypertension and diminished pulse in the lower extremities.

LocalizationJunction of the aortic arch and the descending segment
Upper-extremity pressureIncreased blood pressure
Lower-extremity pressureDecreased blood pressure, weak pulse
CollateralsInternal thoracic and intercostal arteries
3 min readFor medical studentsUpdated Sep 25, 2026
Material prepared by WhiteCoat Pro editorial team based on platform study guidesReviewed by medical editor: Aulov A. A., general practitioner · 09/24/2026

Core anomaly and hemodynamics

The anatomical feature is the formation of a localized narrowing of the vascular bed at the transition of the arch into the descending part. This obstruction to blood flow forces the cardiovascular system to operate under severe compensatory strain.

In response to the blood flow obstruction, left ventricular hypertrophy develops as the heart must overcome increased resistance. Clinically, this manifests as a persistent elevation of blood pressure in the upper extremities, while blood pressure drops and a weakened pulse are recorded in the lower extremities.

Compensatory mechanisms

To ensure perfusion of the lower half of the body under conditions of a narrowed major vessel lumen, the body activates alternative collateral blood supply pathways.

  • The development of collateral circulation occurs via the system of internal thoracic and intercostal arteries.
  • Increased myocardial workload leads to thickening of its walls, resulting in left ventricular hypertrophy.
Test your knowledge on the topicTasks from the "Pathological Anatomy" course bank — instant answers and explanations.

«Blue type» variant

In medical practice, a special variant of the pathology is distinguished, known as the «blue type» variant.

Its development is associated with the embryological shift of the aortopulmonary septum to the left. As a result of this anatomical defect, the pathological process is accompanied by marked left ventricular hypoplasia, while the right ventricle assumes the main load and develops compensatory hypertrophy.

Briefly: answers to topical questions

What anatomical types of aortic coarctation are distinguished in relation to the ductus arteriosus?

The literature describes the following type of coarctation relative to the ductus arteriosus:

  • Infantile type (preductal) — localized proximal to the arterial duct (ductus arteriosus).

In this type, collaterals do not develop prenatally, and after birth, closure of the ductus arteriosus leads to a sharp decrease in blood supply to the distal segments.

What other congenital heart defects are most commonly associated with aortic coarctation?

Aortic coarctation is associated with the following congenital heart defects:

  • Bicuspid aortic valve.
  • Ventricular septal defect (VSD).
  • Hypoplastic left heart syndrome.

In the infantile type, association with other congenital heart defects is noted in 50% of cases, including bicuspid aortic valve, VSD, and hypoplastic left heart syndrome.

What specific radiological signs are characteristic of long-standing aortic coarctation?

Long-standing aortic coarctation is characterized by the following specific radiological signs:

  • Rib notching (rib-notching) — bilateral notches on the inferior margins of the ribs, occurring secondary to the pressure of dilated intercostal arteries during the development of collateral circulation.
  • Alteration of the aortic arch — in the anteroposterior view, the entire region of the arch (aortic knuckle) may appear diminished and flattened.
  • Dilatation of the internal thoracic artery (a. thoracica interna) — visualized behind the sternum in the lateral view.

What life-threatening complications can develop in the natural history of aortic coarctation?

In the natural course of untreated aortic coarctation, fatal outcome is inevitable, driven by the following life-threatening complications:

  • Heart failure — develops in late stages due to left ventricular pressure overload.
  • Aortic rupture and aortic dissection — severe vascular catastrophes.
  • Infective endocarditis — infectious involvement of cardiac structures.
  • Intracerebral hemorrhage — occurs due to the rupture of associated cerebral aneurysms.
How to memorize

Warm top, cold bottom: upper-extremity pressure is elevated, while lower-extremity pressure drops due to narrowing.

Class and exam questions

Where precisely is the narrowing anatomically located in aortic coarctation?

The narrowing is localized in the area of the transition of the aortic arch into its descending part.

Why does blood pressure drop in the lower extremities in this defect?

The drop in pressure and weakening of the pulse in the lower extremities are caused by a mechanical obstruction to blood flow at the site of vascular narrowing.

Which vessels participate in the formation of collateral circulation?

Collateral blood flow develops via the system of internal thoracic and intercostal arteries.

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What else to study on this topic

  • Anatomical features of the blue type variants
  • The role of aortopulmonary septum shift
  • Mechanisms of left ventricular hypoplasia development
  • Hemodynamic differences between the right and left ventricles in this pathology
  • Detailed analysis of collateral blood flow pathways

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