Understand the body’s main artery

Aortic
Disease

The aorta carries blood from the heart to every organ. Aortic disease may remain silent for years, yet an acute aortic event can become life-threatening within minutes.

Explore the aorta
Patient-friendlyEvidence-informedUpdated August 2026
Clinical aortic atlasCTA · MRA · 3D
Clinical CT and MR angiographic images showing an aneurysm involving the distal aortic arch
Thoracic aortic aneurysm on cross-sectional imagingCTA and MRA define the location, morphology, branches and full extent of disease.

Know the anatomy

One continuous artery, several regions.

The location and extent of disease influence surveillance, procedural planning and the team involved in treatment.

Anatomical illustration of the aortic root, ascending aorta and aortic valve
Aortic root and proximal ascending aortaThe aortic valve, coronary origins and root form one functional unit.
01

Aortic root

Connects the left ventricle and aortic valve to the ascending aorta; the coronary arteries originate here.

02

Ascending aorta

Travels upward from the heart before becoming the arch.

03

Aortic arch

Curves over the heart and gives branches to the head and arms.

04

Descending and abdominal aorta

Continues through the chest and abdomen to supply the organs and legs.

Clinical illustration

Anatomical plates and clinical figures are taken from the supplied cardiovascular surgery textbooks—not generated by AI.

Main disease patterns

Different problems require different plans.

Select a condition to view its clinical image and key meaning.

CT and MR angiographic images showing a distal aortic arch aneurysm
Condition 01

Aortic aneurysm

An abnormal enlargement caused by weakening of the aortic wall. It may occur in the chest or abdomen and often causes no symptoms.

Why it mattersRisk depends on location, size, growth, cause and individual characteristics—not one number alone.

Imaging and assessment

Measure consistently. Follow over time.

Echocardiography, CT angiography and cardiac MRI are complementary. The same anatomical level and reproducible technique matter when comparing measurements.

  1. 01
    Clinical and family history

    Symptoms, blood pressure, valve disease, relatives with aneurysm/dissection and syndromic features.

  2. 02
    Define the anatomy

    Identify affected segments, branch involvement and establish a reliable baseline diameter.

  3. 03
    Assess growth and risk

    Repeat imaging at an individualized interval; rapid growth and associated conditions change decisions.

  4. 04
    Multidisciplinary review

    Complex disease benefits from an experienced aortic team including imaging, cardiology, genetics, surgery and endovascular specialists.

Long-term aortic care

Protect the aorta today—and for life.

Surveillance, risk reduction and timely intervention are parts of one continuous plan.

01 · Monitor

Surveillance imaging

Frequency depends on location, size, growth, cause and family history. Keep copies of previous measurements and reports.

Consistency is essential when comparing studies.
02 · Control

Blood pressure and risk

Take prescribed medication, avoid smoking and manage cardiovascular risk factors. Exercise and lifting advice should be individualized.

Ask your clinician for a safe activity plan.
Operative photographs of aortic root and ascending aortic replacement
Operative views of aortic root and ascending aortic replacement.
When intervention is needed

Treatment is tailored to anatomy.

Open repair remains essential for many root, ascending and arch conditions. Endovascular or hybrid repair may be suitable for selected descending and thoracoabdominal disease. The goal is durable exclusion or replacement of the diseased segment while protecting the heart, brain, spinal cord and major branches.

FAMILYDNA
Family matters

Ask whether relatives should be screened.

Genetic counselling and imaging of first-degree relatives may be appropriate when thoracic aortic disease, bicuspid aortic valve or an inherited condition is suspected.

Prepare for your visit

Six useful questions to ask.

01

Which segment of my aorta is affected?

02

What is the maximum diameter and how was it measured?

03

Has the aorta changed compared with previous imaging?

04

Which symptoms require emergency help?

05

Should I modify exercise or heavy lifting?

06

Should my relatives have imaging or genetic assessment?

Frequently asked questions

Clear answers to common concerns.

Can an aortic aneurysm cause no symptoms?+

Yes. Many aneurysms are discovered incidentally. Once disease is identified, planned imaging surveillance is important even when you feel well.

Does every aneurysm need surgery?+

No. Many aneurysms are monitored. Intervention is individualized using symptoms, location, diameter, growth, cause, body size and overall procedural risk.

Can I exercise with aortic disease?+

Regular moderate activity may be appropriate, but advice about heavy isometric exertion and lifting must be tailored to your aortic condition and blood pressure.

Why might my family need testing?+

Some thoracic aortic diseases cluster in families. Identifying relatives at risk allows earlier surveillance and prevention.

What is the difference between an aneurysm and a dissection?+

An aneurysm is enlargement of the aorta. A dissection begins with separation of the aortic wall layers by blood and may occur with or without a pre-existing aneurysm.

For healthcare professionals

Guideline-based aortic care

Management integrates anatomy, phenotype, indexing, growth rate, genetic diagnosis, family history, valve disease, symptoms, procedural expertise and shared decision-making.

Medical disclaimer

This page provides general education and is not a diagnosis or a substitute for consultation with a qualified healthcare professional. Treatment decisions must be individualized.

Clinical sources2024 ESC Guidelines for Peripheral Arterial and Aortic Diseases · 2022 ACC/AHA Guideline for the Diagnosis and Management of Aortic DiseaseIllustration sourcesCarpentier A, Adams DH, Filsoufi F. Carpentier’s Reconstructive Valve Surgery. Saunders Elsevier; 2010. Kofidis T, ed. Minimally Invasive Cardiac Surgery: A Practical Guide. CRC Press; 2021. Chapters 7.2 and 14.2.