Your doctor might check for the condition if he or she hears an abnormal sound in your upper stomach area or your neck that could be caused by the narrowed arteries. If someone in your family has or had fibromuscular dysplasia or aneurysm, your doctor might recommend checking you for the condition, even if you have no signs or symptoms.

Your doctor will perform a physical exam and order blood tests, including blood sugar and cholesterol levels, to check for signs of atherosclerosis, another condition that can narrow your arteries.

Tests to diagnose fibromuscular dysplasia could include:

  • Duplex ultrasound. This noninvasive imaging test can determine if an artery is narrowed. An instrument called a transducer is pressed to your skin to send sound waves into your body. They bounce off cells and body structures, showing how fast your blood flows and the size and shape of the blood vessels.
  • CT angiogram. This test provides cross-sectional images of your body, which can show narrowing in the arteries, aneurysms and dissections. You lie on a narrow table, which slides through a doughnut-shaped scanner. Before the test starts, you'll receive an injection of a dye, which highlights areas of the body being examined.
  • Magnetic resonance (MR) angiogram. This test uses a magnetic field and radio waves to create images of the body. It can see if you have an aneurysm or dissection. During the test, you'll lie on a narrow table that slides into a tubelike machine that's open on both ends. Before the test starts, you might receive an injection of a dye, which highlights areas of the body being examined.
  • Catheter-based angiography. During this commonly used test for fibromuscular dysplasia, a thin tube (catheter) is inserted into one of your arteries and moved until it reaches the area your doctor wants to examine. A tiny amount of dye is injected and X-rays are used to examine the area.

The most common form of fibromuscular dysplasia looks like a "string of beads" on imaging tests. Other forms of fibromuscular dysplasia have a smooth focal appearance.

Once you've been diagnosed with fibromuscular dysplasia, your doctor will follow you clinically. Occasionally, for example if you have an aneurysm, or if your symptoms change, you may need repeat imaging to monitor the arteries.


Treatment for fibromuscular dysplasia depends on the symptoms, the site of the narrowed artery and other health conditions you have, such as high blood pressure. If you don't need treatment at the time, your doctor might recommend watchful waiting.


Treatment with high blood pressure medications is recommended for people with fibromuscular dysplasia who have hypertension, even if they have a procedure to correct the condition. Several types of medications are available:

  • Angiotensin-converting enzyme (ACE) inhibitors, such as benazepril (Lotensin), enalapril (Vasotec) or lisinopril (Prinivil, Zestril), help relax your blood vessels.
  • Angiotensin II receptor blockers. These medications also help relax your blood vessels. Examples of this class of medications include candesartan (Atacand), irbesartan (Avapro), losartan (Cozaar) and valsartan (Diovan).
  • Diuretics. These drugs, such as hydrochlorothiazide (Microzide), help remove excess fluid from your body and may be used with other blood pressure medications.
  • Calcium channel blockers, such as amlodipine (Norvasc), nifedipine (Procardia) and others, help relax your blood vessels.
  • Beta blockers, such as metoprolol (Lopressor), atenolol (Tenormin) and others, slow your heartbeat and block adrenaline.

Your doctor might advise you take a daily aspirin to reduce your risk of stroke. But don't start taking an aspirin without talking to your doctor first.

Some medications used to treat hypertension can affect the way your kidneys work. Your doctor might recommend blood and urine tests to make sure your kidneys are working normally once you start taking these medications.

Surgery or other procedures

Percutaneous transluminal angioplasty (PTA)

This procedure is preferred over surgery and is usually done at the same time as a catheter-based angiogram. During an angiogram, dye is injected through a catheter into an artery. X-rays show how the dye travels through the artery, revealing narrowed areas. A wire is threaded to the artery, and a catheter with a balloon is inserted into the narrowed area.

The balloon is then inflated to open the narrowed part of the artery. Rarely, a metal mesh tube (stent) may be placed inside the weakened part of the artery to help prevent it from rupturing.

Surgical revascularization

Surgery to repair the damaged artery is rarely recommended. It's usually only done when there are complications. However, if PTA is not an option and the narrowing of your arteries is severe, your doctor might recommend a more invasive approach with surgery to repair or replace the narrowed portion of the artery. The type of surgery depends on the site of the narrowed artery and how damaged the artery is.

Clinical trials

Explore Mayo Clinic studies testing new treatments, interventions and tests as a means to prevent, detect, treat or manage this condition.

Preparing for your appointment

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

What you can do

When you make the appointment, ask if there's anything you need to do in advance. For example, you might need to fast for several hours before the tests. Also, bring a family member or friend to your appointment, if possible, to help you remember the information you're given.

Make a list of:

  • Your symptoms and when they began
  • Key personal information, including a family history of fibromuscular dysplasia, aneurysms, heart disease, stroke or high blood pressure
  • All medications, vitamins or other supplements you take, including doses
  • Questions to ask your doctor

For fibromuscular dysplasia, some basic questions to ask your doctor include:

  • What's the most likely cause of my symptoms?
  • What tests will I need?
  • What treatments are available? What do you recommend for me?
  • What's an appropriate level of physical activity?
  • How often should I be monitored for fibromuscular dysplasia?
  • I have other health conditions. How can I best manage these conditions together?
  • Should I see a specialist?
  • Are there brochures or other printed material that I can have? What websites do you recommend?

Don't hesitate to ask other questions.

What to expect from your doctor

Your doctor is likely to ask you questions, such as:

  • Have your symptoms been continuous or occasional?
  • How severe are your symptoms?
  • Does anything seem to improve your symptoms?
  • What, if anything, appears to worsen your symptoms?

Fibromuscular dysplasia care at Mayo Clinic

Aug. 12, 2021
  1. Olin JW. Clinical manifestations and diagnosis of fibromuscular dysplasia. https://www.uptodate.com/contents/search. Accessed March 26, 2021.
  2. Fibromuscular dysplasia information page. National Institute of Neurological Disorders and Stroke. https://www.ninds.nih.gov/disorders/all-disorders/fibromuscular-dysplasia-information-page. Accessed March 26, 2021.
  3. Masoura C, et al. Think of fibromuscular dysplasia whenever spontaneous coronary artery dissection presents. Hellenic Journal of Cardiology. 2020; doi:10.1016/j.hjc.2019.10.014.
  4. AskMayoExpert. Fibromuscular dysplasia. Mayo Clinic; 2020.
  5. Olin JW. Treatment of fibromuscular dysplasia of the renal arteries. https://www.uptodate.com/contents/search. Accessed March 26, 2021.
  6. Gornik HL, et al. First international consensus on the diagnosis and management of fibromuscular dysplasia. Vascular Medicine. 2019; doi:10.1177/1358863X18821816.
  7. Riggin EA. Allscripts EPSi. Mayo Clinic. March 26, 2021.


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