Giant cell arteritis

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(Redirected from Horton disease)

Giant cell arteritis (GCA), also known as temporal arteritis and cranial arteritis, is an inflammatory disease of blood vessels. Most commonly, it affects the arteries of the head, especially those in the temples. For this reason, it is often called temporal arteritis. If the disease is not treated, it can lead to blindness or stroke.

Symptoms[edit | edit source]

The most common symptoms of giant cell arteritis are head pain and tenderness — often severe — that usually affects both temples. Other signs and symptoms, which can occur suddenly, include:

Causes[edit | edit source]

The exact cause of giant cell arteritis is unknown. It is thought that a combination of genetic and environmental factors, such as infections, play a role. The condition is related to an abnormal immune response.

Diagnosis[edit | edit source]

Diagnosis of giant cell arteritis can be difficult because the symptoms are similar to those of other conditions. However, a biopsy of the temporal artery can confirm the diagnosis. Other tests, such as blood tests and imaging studies, may also be used.

Treatment[edit | edit source]

Treatment for giant cell arteritis involves high doses of a corticosteroid drug such as prednisone. Because of the risk of vision loss, treatment typically begins as soon as the disease is suspected, even before a diagnosis is confirmed.

Prognosis[edit | edit source]

With early diagnosis and treatment, the prognosis for people with giant cell arteritis is generally good. However, relapses are common and long-term medication may be needed.

See also[edit | edit source]

References[edit | edit source]

Giant cell arteritis Resources
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Contributors: Prab R. Tumpati, MD