Most thoracic aortic aneurysms are smaller and develop slowly
Q: What causes a thoracic aortic aneurysm? Does it always grow slowly, or do some develop more quickly?
A: A thoracic aortic aneurysm occurs when one or more areas along the wall of the aorta — the body’s largest blood vessel — becomes weak or damaged. The aorta carries oxygen-filled blood from the heart to the body, including the brain. With time, the pressure of blood flowing through the weakened area can cause it to enlarge or bulge — typically without signs or symptoms.
Most commonly, bulges occur in the abdomen (abdominal aortic aneurysm). However, aneurysms also may develop closer to the heart in the chest area (thoracic aortic aneurysm).
The main concern with aortic aneurysms is a tear, or dissection, or, more seriously, a rupture that allows blood to leak into the aorta’s lining or into the body. With a dissection or rupture, it’s important to quickly recognize these symptoms: sharp, severe or sudden chest or upper back pain that radiates downward, or includes the jaw, neck or arms; difficulty breathing or swallowing; and clamminess. Immediate emergency care, including open-chest surgery, is necessary for a dissection or rupture. Unfortunately, both dissections and ruptures are often fatal.
Most aortic aneurysms are small and develop slowly. They are discovered when imaging is performed on the chest or abdominal area for another reason.
A smaller aneurysm has a low risk of rupture — about 1% or less per year. For that reason, as long as
it’s not growing quickly, most health care providers will recommend a watchand-wait approach. This means using imaging tests, such as ultrasound, at regular intervals to monitor the aneurysm’s size and rate of growth. Providers also may prescribe medications such as beta blockers. These are used to treat high blood pressure, which is present in about 60% of people with thoracic aortic aneurysms.
An aneurysm can grow faster, particularly in people with a family history of aortic aneurysms or with a genetic condition related to the body’s connective tissues. If an aneurysm is larger or found to be growing too quickly, elective surgery to repair the aneurysm may be considered. This usually involves openchest surgery to remove the damaged section of the aorta and replace it with a synthetic tube, or graft. In select cases, repair with endovascular surgery using small incisions and surgical instruments inserted through catheters may be necessary.
Men are much more likely than women to develop a thoracic aortic aneurysm. Most
commonly, the condition starts to occur in people in their 50s and 60s, although it may not be detected until decades later, if at all.
Genetic connective tissue disorders — Marfan, Ehlers-Danlos and Loeys-Dietz syndromes — dramatically increase your risk. Those born with just two, rather than three, leaflets (cusps) of the aortic valve — a condition called bicuspid aortic valve — are at increased risk.
Other factors that increase the risk include high blood pressure, smoking, undesirable cholesterol levels, and development of blood vessel hardening and clogging, or atherosclerosis.
People at highest risk — those with a family history plus one or more other risk factors — should ask their health care provider about having an echocardiogram to look for a thoracic aneurysm, even in the absence of signs or symptoms.
Mayo Clinic Q& A is an educational resource and doesn’t replace regular medical care. Email a question to MayoClinic Q& A@mayo.edu.