Condition guide
Thoracic aortic aneurysm: causes and treatment
A thoracic aortic aneurysm is a swelling or bulge in the part of the aorta that runs through the chest. Most are small, grow slowly and cause no symptoms, so they are often found by chance during a scan done for another reason. The aim of care is to watch the size, control blood pressure and other risks, and offer repair before a tear or rupture can occur.
Last checked: 2026-10-04
Key facts
At a glance.
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What it is
The British Heart Foundation describes a swelling or bulging of the aorta in the chest, usually where the wall has become weak and has lost its elasticity.
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Usually silent
BHF says thoracic aortic aneurysms are often small, grow slowly and most of the time have no symptoms. Patient.info professional reference puts this at about 95%.
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Who is at risk
BHF lists smoking, high blood pressure, family history, older age (most often 65 and over) and genetic conditions such as Marfan syndrome, Loeys-Dietz syndrome and vascular Ehlers-Danlos syndrome.
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Monitoring
BHF says it is likely you will be monitored with echocardiograms and CT scans every 6 or 12 months to look for changes.
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Emergency signs
Sharp, sudden pain in the upper back that spreads downward, chest, jaw, neck or arm pain, difficulty breathing or collapse need a 999 call.
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Normal life
BHF says most people can still live a normal life, with regular tests and advice to avoid heavy lifting and some physical activities.
What a thoracic aortic aneurysm is
The aorta is the main artery carrying oxygen-rich blood from the heart to the rest of the body. The thoracic part runs through the chest. Leeds Teaching Hospitals explains that it is measured at six points along its course, and that an aneurysm is an enlargement to 1.5 times the expected diameter at one or more of them.
The wall of a healthy aorta is strong and elastic. BHF says that in an aneurysm the wall has weakened and lost its elasticity, so it does not return to shape after the blood has passed through. Patient.info says it can involve the ascending aorta, the arch, the descending aorta or the thoracoabdominal aorta.
The danger is a tear between the layers of the wall, called aortic dissection, or a rupture. BHF says dissection can be life-threatening if not treated immediately. Depending on size and growth, many aneurysms never burst or tear.
Causes and risk factors
BHF lists several causes: atherosclerosis, high blood pressure, high cholesterol, genetic conditions, a congenital problem with the aorta or aortic valve, blood vessel inflammation such as giant cell arteritis or Takayasu arteritis, rarely untreated infection such as syphilis, and traumatic injury. It adds that aneurysms in younger people often have a genetic cause.
Patient.info names high blood pressure as the major risk factor for thoracic aortic disease. It also lists increasing age, smoking, high lipids, bicuspid aortic valves, sleep apnoea, chronic kidney disease and cocaine use. It notes weightlifting and stimulants may contribute through large rises in blood pressure.
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High blood pressure and smoking
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Atherosclerosis and high cholesterol
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Marfan, Loeys-Dietz and vascular Ehlers-Danlos syndromes
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A bicuspid aortic valve or other congenital aortic problem
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Inflammation of the aorta, for example from giant cell arteritis
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Family history of aortic aneurysm or dissection
Symptoms
As a thoracic aortic aneurysm grows, BHF says symptoms may include back pain, cough, a weak, scratchy voice, shortness of breath and tenderness or pain in the chest. Leeds Teaching Hospitals adds pain in the jaw, a hoarse voice, and difficulty breathing or swallowing for larger aneurysms. These come from pressure on nearby structures.
A bursting or tearing aneurysm is an emergency. BHF lists sharp, sudden pain in the upper back that spreads downward, pain in the chest, jaw, neck or arms, difficulty breathing, very low blood pressure, trouble swallowing and loss of consciousness. Patient.info says dissection typically brings sudden, very severe, tearing pain at its maximum from the start, unlike the building pain of a heart attack.
How it is found and followed up
BHF says thoracic aortic aneurysms are often found when a test is done for something else. Tests used include chest X-ray, ECG, echocardiogram, cardiac CT scan and cardiac MRI scan. Patient.info says CT with contrast is the most widely used diagnostic tool and that echocardiography shows the aortic valve and root.
BHF notes that aortic conditions can be inherited. If a close relative has had an aortic aneurysm you should speak to your doctor about screening for you and your family. Genetic testing is available for aortic conditions and is recommended through an inherited cardiac clinic. Leeds Teaching Hospitals says relatives may be invited for assessment by a clinical genetics team.
Once an aneurysm is known, scans are repeated at intervals so changes in size can be seen early. BHF says how fast the aneurysm grows, if at all, differs for everyone.
| Test | What it adds |
|---|---|
| Chest X-ray | May show a widened aorta, often found by chance |
| Echocardiogram | Shows the aortic root and valve |
| CT scan | Gives a detailed size and shape of the whole thoracic aorta |
| MRI scan | Detailed images without X-ray radiation |
| Genetic testing | Looks for inherited causes, via an inherited cardiac clinic |
Treatment: monitoring, medicines and surgery
BHF says treatment varies from regular health checks to emergency surgery, depending on cause, size, location and growth rate. Leeds Teaching Hospitals says treatment is tailored and considers size, cause, medical history and your preferences. It offers regular scans, medicines to lower blood pressure which have been shown to slow aortic enlargement, and family screening where genetics may be involved.
BHF lists medicines used to control risk factors, including angiotensin receptor blockers, beta blockers and statins. Patient.info says rigorous blood pressure control, stopping smoking and treating other cardiovascular risks are central.
Surgery is considered when the aneurysm has grown too much, causes symptoms, or in Marfan syndrome. BHF describes replacing the section of aorta with a synthetic graft. Other options are stent-based repair and, for some people with Marfan syndrome, a custom support sleeve around the aortic root. Patient.info says symptomatic aneurysms merit repair regardless of size, and that people with Marfan syndrome or a strong family history are operated on at a smaller size.
Living with an aneurysm: exercise and lifestyle
BHF says your doctor may advise avoiding heavy lifting and some physical activities that can raise blood pressure and strain the aneurysm. Leeds Teaching Hospitals separates dynamic exercise such as walking, which changes heart rate and blood pressure gradually, from static or explosive exercise such as weight lifting or sprinting, which causes sudden changes. It advises avoiding static exercise and contact sports, and discussing any new activity with your doctor.
Lifestyle measures from the same leaflet include a diet low in saturated fat, not smoking, keeping alcohol to 14 units a week or less and a healthy weight, all of which help lower blood pressure. If you may become pregnant, ask about family planning advice, since a dilated aorta can have a genetic cause.
When to get emergency help
BHF says that if you have sudden sharp upper back pain that spreads downward, chest, jaw, neck or arm pain, difficulty breathing, trouble swallowing or loss of consciousness, you or someone else should call 999 immediately.
If you have a known aneurysm and notice new chest or back pain, a hoarse voice, a cough that does not go away, or difficulty swallowing, contact your specialist team or GP promptly. Do not assume it is a pulled muscle.
NHS pathway and private specialists
Aneurysms are usually found incidentally and referred to cardiology, cardiothoracic or vascular teams. Some hospitals run dedicated aortopathy clinics, as Leeds does. Surgical planning includes a pre-operation clinic, blood tests and imaging.
Private cardiologists and cardiothoracic surgeons also see people for scans, surveillance and second opinions. Whoever you see, ask which measurement is being tracked, when the next scan is due, and at what size repair would be discussed for you.
Frequently asked
Questions people ask.
Quick, plain-English answers to the questions we hear most.
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What is the difference between an aneurysm and a dissection?
An aneurysm is a widening of the aorta. A dissection is a tear between the layers of its wall. BHF says dissection can be life-threatening if not treated immediately.
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Will I feel it?
Usually not. BHF says most thoracic aortic aneurysms have no symptoms. Symptoms such as back pain, cough or a hoarse voice tend to appear as they grow.
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How often are scans needed?
BHF says it is likely to be every 6 or 12 months. Patient.info mentions CT or MRI about every 6 months in some situations. Your team will set the interval.
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Can I exercise?
Usually yes, with limits. Leeds Teaching Hospitals favours walking-type exercise and advises avoiding static exercise such as weight lifting and contact sports. Check with your doctor first.
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Is it hereditary?
Sometimes. BHF says aortic conditions can be inherited and that aneurysms in younger people often have a genetic cause. Family screening may be offered.
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Which medicines are used?
BHF lists angiotensin receptor blockers, beta blockers and statins to control blood pressure and cholesterol. Leeds Teaching Hospitals says blood pressure-lowering medicine has been shown to slow aortic enlargement.
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When is surgery recommended?
BHF says when the aneurysm has grown too much, causes symptoms, or in Marfan syndrome. The exact size depends on the individual, so your surgeon will explain the threshold for you.
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What operation is used?
BHF describes replacing the affected section with a synthetic graft, stent-based repair, and a custom support sleeve in some people with Marfan syndrome.
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Can untreated syphilis cause one?
Rarely. BHF lists untreated infection such as syphilis or salmonella among possible causes, and Patient.info lists tertiary syphilis too.
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Can I drive or fly with one?
This depends on your size, symptoms and any DVLA rules. Ask your specialist rather than relying on general advice, as the answer is individual.
Where this comes from
Sources and checking.
This guide is for information, not medical advice.
Your GP or consultant knows your history and can tell you which parts apply to you. If your symptoms are severe, rapidly worsening, or come with red-flag features, seek urgent medical care. Figures and availability change, so treat them as a guide and confirm with the provider.
Published 2026-10-04, next review 2027-10-04.
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British Heart Foundation: Thoracic aortic aneurysm, https://www.bhf.org.uk/informationsupport/conditions/thoracic-aortic-aneurysm, retrieved October 2026
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Leeds Teaching Hospitals NHS Trust: Leeds Aortopathy Clinic and Thoracic Aortic Aneurysms, https://www.leedsth.nhs.uk/patients/resources/leeds-aortopathy-clinic-and-thoracic-aortic-aneurysms-taa/, retrieved October 2026
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Patient.info professional reference: Thoracic aortic aneurysms, https://patient.info/doctor/cardiovascular-disease/thoracic-aortic-aneurysms, retrieved October 2026
Related guides
Keep reading.
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Aortic aneurysm
Overview including the abdominal aorta
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Aneurysms
Aneurysms in different parts of the body
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Marfan syndrome
An inherited cause of aortic widening
Read guide -
Marfan aortic surveillance
How the aorta is followed in Marfan syndrome
Read guide -
Loeys-Dietz syndrome
A genetic condition linked to aortic aneurysm
Read guide -
Giant cell arteritis
Inflammation that can involve the aorta
Read guide -
Cardiothoracic surgery department
Surgical repair of the aorta
Read guide -
Cardiology department
Imaging and long-term surveillance
Read guide