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Takayasu’s arteritis

Takayasu arteritis (tah-kah-YAH-soo ahr-tuh-RIE-tis) is a rare type of vasculitis. Vasculitis is a group of conditions that causes blood vessel swelling, called inflammation. In Takayasu arteritis, the swelling damages the large artery that carries blood from the heart to the rest of the body, called the aorta, and its main branches.

The condition can narrow or block arteries. The artery walls may bulge and tear, called an aneurysm. It also can cause arm or chest pain and high blood pressure. In time, Takayasu arteritis can cause heart failure or stroke.

People who don’t have symptoms may not need treatment. But most people with the condition need medicines to control inflammation in the arteries and prevent complications. Even with treatment, the condition often comes back. And symptoms may come and go.

The symptoms of Takayasu arteritis often come in two stages.

Stage 1

In the first stage, you’re likely to feel not well. Symptoms may include:

Not everyone has these early symptoms. Inflammation can harm arteries for years before symptoms begin.

Stage 2

During the second stage, the swelling causes arteries to narrow. Less blood and oxygen reach the organs and tissues. Stage 2 symptoms may include:

Seek medical help right away for shortness of breath, chest or arm pain, or signs of a stroke. Signs of a stroke include face drooping, arm weakness or having trouble speaking.

Make an appointment with your healthcare professional if you have symptoms that worry you. Finding Takayasu arteritis early is key to treating it.

If you’ve been diagnosed with Takayasu arteritis, your symptoms may come and go even with treatment. Watch for symptoms you had at the start of the condition or any new ones. Tell your healthcare professional right away about any changes.

No one knows exactly what causes the first swelling, called inflammation, in Takayasu arteritis. It’s likely an autoimmune condition. This means the immune system attacks the arteries by mistake. A virus or other infection may set off the condition.

Takayasu arteritis mainly affects people assigned female at birth who are younger than 40. The condition happens around the world. But it’s most common in Asia.

Sometimes the condition runs in families. Researchers have found certain genes that are linked with Takayasu arteritis.

With Takayasu arteritis, cycles of swelling and healing in the arteries might lead to one or more of these complications:

Pregnancy

People with Takayasu arteritis can have a healthy pregnancy. But the condition and medicines that treat it can affect being able to get pregnant and the pregnancy.

If you have Takayasu arteritis and plan to get pregnant, work with your healthcare professional before you get pregnant to make a plan to limit complications of pregnancy. See your healthcare team regularly during your pregnancy.

Your healthcare professional asks you about your symptoms, does a physical exam, and takes your medical history. You also may have some tests and procedures. They can help confirm the diagnosis and rule out other conditions that are like Takayasu arteritis. Some of these tests also may be used to check your progress during treatment.

Tests and procedures might include:

Treatment of Takayasu arteritis aims at controlling inflammation with medicines and preventing more damage to the blood vessels.

Takayasu arteritis can be hard to treat. The condition can stay active even if symptoms improve. It’s also possible that you already have damage that can’t be fixed by the time you’re diagnosed.

If you don’t have symptoms or serious complications, you may not need treatment. Or your healthcare professional may have you taper and stop treatment over time.

Medicines

Talk with your healthcare professional about what medicines you might take and their possible side effects. Medicines may include:

手術

For very narrow arteries, surgery can open or go around, called bypass, these arteries to allow blood to flow better. Often this helps improve certain symptoms, such as high blood pressure and chest pain. But sometimes, the narrowing or blockage may happen again. This needs a second procedure.

Also, surgery may prevent large aneurysms from tearing.

It’s best to have surgery after the swelling in the arteries has gone down. Surgical options include:

One of the hardest things about living with Takayasu arteritis may be coping with side effects of medicine. The following tips may help:

For Takayasu arteritis, your main healthcare professional may send you to one or more specialists in helping people with this condition. Takayasu arteritis is a rare condition that can be hard to diagnose and treat.

You may want to talk with your healthcare professional about sending you to a medical center that specializes in treating vasculitis.

Here’s some information to help you get ready for your appointment.

What you can do

When you make the appointment, ask if you need to do anything before it, such as restrict your diet. Ask a family member or friend to go with you to help you keep track of what you learn during your visit.

Make a list of:

For Takayasu arteritis, some questions to ask include:

What to expect from your doctor

Questions your healthcare professional might ask include:

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