Giant Cell Arteritis
Giant cell arteritis is an inflammation of the lining of your arteries. Most often, it affects the arteries in your head, especially those in your temples. For this reason, giant cell arteritis is sometimes called temporal arteritis.
Giant cell arteritis frequently causes headaches, scalp tenderness, jaw pain and vision problems. Untreated, it can lead to blindness.
Prompt treatment with corticosteroid medications usually relieves symptoms of giant cell arteritis and might prevent loss of vision. You’ll likely begin to feel better within days of starting treatment. But even with treatment, relapses are common.
You’ll need to visit your doctor regularly for checkups and treatment of any side effects from taking corticosteroids.
The most common symptoms of giant cell arteritis are head pain and tenderness — often severe — that usually affects both temples. Head pain can progressively worsen, come and go, or subside temporarily.
Generally, signs and symptoms of giant cell arteritis include:
- Persistent, severe head pain, usually in your temple area
- Scalp tenderness
- Jaw pain when you chew or open your mouth wide
- Fever
- Fatigue
- Unintended weight loss
- Vision loss or double vision, particularly in people who also have jaw pain
- Sudden, permanent loss of vision in one eye
Pain and stiffness in the neck, shoulders or hips are common symptoms of a related disorder, polymyalgia rheumatica. About 50 percent of people with giant cell arteritis also have polymyalgia rheumatica.
When to see a doctor
If you develop a new, persistent headache or any of the signs and symptoms listed above, see your doctor without delay. If you’re diagnosed with giant cell arteritis, starting treatment as soon as possible can usually help prevent vision loss.
With giant cell arteritis, the lining of arteries becomes inflamed, causing them to swell. This swelling narrows your blood vessels, reducing the amount of blood — and, therefore, oxygen and vital nutrients — that reaches your body’s tissues.
Almost any large or medium-sized artery can be affected, but swelling most often occurs in the arteries in the temples. These are just in front of your ears and continue up into your scalp.
What causes these arteries to become inflamed isn’t known, but it’s thought to involve abnormal attacks on artery walls by the immune system. Certain genes and environmental factors might increase your susceptibility to the condition.
Several factors can increase your risk of developing giant cell arteritis, including:
- Age. Giant cell arteritis affects adults only, and rarely those under 50. Most people with this condition develop signs and symptoms between the ages of 70 and 80.
- Sex. Women are about two times more likely to develop the condition than men are.
- Race and geographic region. Giant cell arteritis is most common among white people in Northern European populations or of Scandinavian descent.
- Polymyalgia rheumatica. Having polymyalgia rheumatica puts you at increased risk of developing giant cell arteritis.
- Family history. Sometimes the condition runs in families.
Giant cell arteritis can cause serious complications, including:
- Blindness. Diminished blood flow to your eyes can cause sudden, painless vision loss in one or, rarely, both eyes. Loss of vision is usually permanent.
Aortic aneurysm. An aneurysm is a bulge that forms in a weakened blood vessel, usually in the large artery that runs down the center of your chest and abdomen (aorta). An aortic aneurysm might burst, causing life-threatening internal bleeding.
Because this complication can occur even years after the diagnosis of giant cell arteritis, your doctor might monitor your aorta with annual chest X-rays or other imaging tests, such as ultrasound and CT.
- Stroke. This is an uncommon complication of giant cell arteritis.
Giant cell arteritis can be difficult to diagnose because its early symptoms resemble those of other common conditions. For this reason, your doctor will try to rule out other possible causes of your problem.
In addition to asking about your symptoms and medical history, your doctor is likely to perform a thorough physical exam, paying particular attention to your temporal arteries. Often, one or both of these arteries are tender, with a reduced pulse and a hard, cordlike feel and appearance.
Your doctor might also recommend certain tests.
Blood tests
The following tests might be used to help diagnose your condition and to follow your progress during treatment.
- Erythrocyte sedimentation rate. Commonly referred to as the sed rate, this test measures how quickly red blood cells fall to the bottom of a tube of blood. Red cells that drop rapidly might indicate inflammation in your body.
- C-reactive protein (CRP). This measures a substance your liver produces when inflammation is present.
Imaging tests
These might be used to diagnose giant cell arteritis and to monitor your response to treatment. Tests might include:
- Doppler ultrasound. This test uses sound waves to produce images of blood flowing through your blood vessels.
- Magnetic resonance angiography (MRA). This test combines an MRI with the use of a contrast material that produces detailed images of your blood vessels. Let your doctor know ahead of time if you’re uncomfortable being confined in a small space because the test is conducted in a tube-shaped machine.
- Positron emission tomography (PET). If your doctor suspects you might have giant cell arteritis in large arteries, such as your aorta, he or she might recommend PET. This test uses an intravenous tracer solution that contains a tiny amount of radioactive material. A PET scan can produce detailed images of your larger blood vessels and highlight areas of inflammation.
Biopsy
The best way to confirm a diagnosis of giant cell arteritis is by taking a small sample (biopsy) of the temporal artery. This artery is situated close to the skin just in front of your ears and continues up to your scalp. The procedure is performed on an outpatient basis using local anesthesia, usually with little discomfort or scarring. The sample is examined under a microscope in a laboratory.
If you have giant cell arteritis, the artery will often show inflammation that includes abnormally large cells, called giant cells, which give the disease its name. It’s possible to have giant cell arteritis and have a negative biopsy result.
If the results aren’t clear, your doctor might advise another temporal artery biopsy on the other side of your head.
The main treatment for giant cell arteritis consists of high doses of a corticosteroid drug such as prednisone. Because immediate treatment is necessary to prevent vision loss, your doctor is likely to start medication even before confirming the diagnosis with a biopsy.
You’ll likely begin to feel better within a few days of beginning treatment. If you have visual loss before starting treatment with corticosteroids, it’s unlikely that your vision will improve. However, your unaffected eye might be able to compensate for some of the visual changes.
You may need to continue taking medication for one to two years or longer. After the first month, your doctor might gradually begin to lower the dosage until you reach the lowest dose of corticosteroids needed to control inflammation.
Some symptoms, particularly headaches, may return during this tapering period. This is the point at which many people also develop symptoms of polymyalgia rheumatica. Such flares can usually be treated with slight increases in the corticosteroid dose. Your doctor might also suggest an immune-suppressing drug called methotrexate (Trexall).
Corticosteroids can lead to serious side effects, such as osteoporosis, high blood pressure and muscle weakness. To counter potential side effects, your doctor is likely to monitor your bone density and might prescribe calcium and vitamin D supplements or other medications to help prevent bone loss.
The Food and Drug Administration recently approved tocilizumab (Actemra) to treat giant cell arteritis. It’s given as an injection under your skin. Side effects include making you more prone to infections. More research is needed.
References
- Docken WP, et al. Clinical manifestations of giant cell arteritis. https://www.uptodate.com/contents/search. Accessed Sept. 7, 2018.
- Patient fact sheet: Giant cell arteritis. American College of Rheumatology. https://www.rheumatology.org/I-Am-A/Patient-Caregiver/Diseases-Conditions/Giant-Cell-Arteritis. Accessed Sept. 7, 2018.
- Docken WP. Diagnosis of giant cell arteritis. https://www.uptodate.com/contents/search. Accessed Sept. 7, 2018.
- Giant cell arteritis. Arthritis Foundation. https://www.arthritis.org/about-arthritis/types/giant-cell-arteritis/. Accessed Sept. 7, 2018.
- Dejaco C, et al. Giant cell arteritis and polymyalgia rheumatic: Current challenges and opportunities. Nature Reviews Rheumatology. 2017;13:578.
- Giant cell arteritis. Genetic and Rare Diseases Information Center. https://rarediseases.info.nih.gov/diseases/9615/giant-cell-arteritis. Accessed Sept. 7, 2018.
- FDA approves Genentech’s Actemra for giant cell arteritis. Vasculitis Foundation. https://www.vasculitisfoundation.org/fda-approves-genentechs-actemra-for-giant-cell-arteritis/. Accessed Sept. 11, 2018.
- Giant cell arteritis. Merck Manual Professional Version. https://www.merckmanuals.com/professional/musculoskeletal-and-connective-tissue-disorders/vasculitis/giant-cell-arteritis. Accessed Sept. 11, 2018.
- What is osteoporosis? NIH Osteoporosis and Related Bone Diseases National Resource Center. https://www.bones.nih.gov/health-info/bone/osteoporosis/osteoporosis-ff. Accessed Sept. 11, 2018.
- Docken WP. Treatment of giant cell arteritis. https://www.uptodate.com/contents/search. Accessed Sept. 7, 2018.
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