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Brain Health > Related Conditions > Giant Cell Arteritis
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Giant Cell Arteritis

(Inflamed Arteries · Temporal Arteritis)


In this condition factsheet:


The Facts on Giant Cell Arteritis

Giant cell arteritis (GCA) is a common inflammation disease of medium- to large-sized arteries. These arteries can become narrowed, restricting blood flow to affected parts of the body. Giant cells are immune cells found in high concentrations inside affected arteries.

Arteries in the head are the most commonly affected, but arteries in the chest, neck, heart, and other parts of the body may also be involved. When the arteries in the temples of the head are affected, it is termed temporal arteritis or cranial arteritis.

There are 3 patterns seen in giant cell arteritis:

  • primarily affecting the head
  • primarily affecting the larger vessels of the chest and neck
  • a wasting, generalized disease

GCA is unusual in people under 50 years of age. The average age for it to start at is 70. Giant cell arteritis affects women more than men. People of African descent are less commonly affected compared to Caucasians.

GCA is closely associated with a disease called polymyalgia rheumatica (PMR), which many experts believe is a different manifestation of the same underlying disorder. About 10% to 20% of people with PMR develop GCA.

About 50% of people with GCA also have the symptoms of PMR. Fortunately, the same treatment is effective for both conditions, but GCA requires much higher doses.

Causes of Giant Cell Arteritis

GCA is an autoimmune disease in which the body's immune system mistakenly attacks the person's own tissue. Autoimmune diseases in general are poorly understood. They tend to run in families, but not so much that we can say they're inherited or genetic diseases. Many doctors believe it takes a combination of predisposing genes and environmental factors to trigger the condition.

Symptoms and Complications of Giant Cell Arteritis

Early symptoms of GCA include fever, weakness, sweating, and weight loss, which may come on suddenly. These symptoms may go on to the classic symptoms of GCA, such as:

  • double vision or blurred vision, or a black curtain coming over vision; these symptoms are due to narrowing of the main artery to the eye
  • headache in the temple or back of the head (over 70% of people have this symptom)
  • sensitive, tender scalp
  • swollen, bumpy, tender arteries in the temple, often lacking a noticeable pulse
  • weakness or pain in the jaw muscles or tongue – lack of oxygen to jaw muscles from chewing brings on pain that goes away when stopped
  • weight loss
  • fever
  • anemia and other blood abnormalities
  • fatigue

If arteritis is left untreated, it can progress to the following symptoms:

  • blind spots or sudden blindness in one eye
  • stroke
  • heart attack
  • other serious conditions due to impaired blood flow in the arteries

Blindness is a serious threat in arteritis. In a few cases, vision loss is the first sign of GCA. Unfortunately, any damage already done is usually irreversible. Most people get warning symptoms (called prodromes), such as fluctuating vision, black curtains that briefly descend over vision in one eye (called amaurosis fugax), and headaches, giving them time to take action and see their doctor.

At least 50 % of GCA patients also have polymyalgia rheumatica (PMR). About 10% to 20% of people with PMR go on to develop GCA. Arteritis may appear before, during, or after the onset of PMR. The primary symptoms of PMR are severe stiffness and pain in the neck, shoulder, and hip muscles. There may also be fatigue, joint pain, joint swelling in the hands, and anemia.



 

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