Giant cell arteritis involves predominantly the thoracic aorta, large arteries emerging from the aorta in the neck, and extracranial branches of the carotid arteries. Simultaneous polymyalgia rheumatica is common. Symptoms and signs may include headaches, visual disturbances, temporal artery tenderness, and pain in the jaw muscles during chewing. Fever, weight loss, malaise, and fatigue are also common. ESR and C-reactive protein are typically elevated. Diagnosis is clinical and confirmed by temporal artery biopsy. Treatment with high-dose corticosteroids and aspirin is usually effective and prevents vision loss.
Giant cell arteritis is a relatively common form of vasculitis in the US and Europe. Incidence varies depending on ethnic background. Autopsy studies suggest that the disorder may be more common than is clinically apparent. Women are affected more often. Mean age at onset is about 70, with a range of 50 to > 90. About 40 to 60% of patients with giant cell arteritis have polymyalgia rheumatica (see Polymyalgia Rheumatica). The intracranial vessels are usually not affected.
Vasculitis may be localized, multifocal, or widespread. The disorder tends to affect arteries containing elastic tissue, most often the temporal, cranial, or other carotid system arteries. The aortic arch branches, coronary arteries, and peripheral arteries can also be affected. Mononuclear cell infiltrates in the adventitia form granulomas containing activated T cells and macrophages. Multinucleated giant cells, when present, cluster near the disrupted elastic lamina. The intimal layer is markedly thickened, with concentric narrowing and occlusion of the lumen.
Symptoms and Signs
Symptoms may begin gradually over several weeks or abruptly.
Patients may present with systemic symptoms such as fever (usually low-grade), fatigue, malaise, unexplained weight loss, and sweats. Some patients are initially diagnosed as having FUO. Eventually, most patients develop symptoms related to the affected arteries.
Severe, sometimes throbbing headache (temporal, occipital, frontal, or diffuse) is the most common symptom. It may be accompanied by scalp pain elicited by touching the scalp or combing the hair.
Visual disturbances include diplopia, scotomas, ptosis, blurred vision, and loss of vision (which is an ominous sign). Brief periods of partial or complete vision loss (amaurosis fugax) in one eye may be rapidly followed by permanent irreversible loss of vision. If untreated, the other eye may also be affected. However, complete bilateral blindness is uncommon. Vision loss is caused by arteritis of branches of the ophthalmic artery or posterior ciliary arteries, which leads to ischemia of the optic nerve. Funduscopic findings may include ischemic optic neuritis with pallor and edema of the optic disk, scattered cotton-wool patches, and small hemorrhages. Later, the optic nerve atrophies. Rarely, central blindness results from infarction in the occipital cortex caused by arterial lesions in the distal cervical region or base of the brain.
Intermittent claudication (ischemic muscle pain) may occur in jaw muscles and muscles of the tongue or extremities. Jaw claudication is noted especially when firm foods are chewed.
Neurologic manifestations, such as strokes and transient ischemic attacks, can result when the carotid or vertebrobasilar arteries or branches are narrowed or occluded.
Thoracic aortic aneurysms and dissection of the aorta are serious, often late, complications.
Giant cell arteritis is suspected in patients > 55 if any of the following develops, especially if they also have symptoms of systemic inflammation:
The diagnosis is more likely if patients also have symptoms of polymyalgia rheumatica.
Physical examination may detect swelling and tenderness, with or without nodularity or erythema, over the temporal arteries. Temporal arteries can become prominent. A temporal artery that rolls under the examiner's fingers, rather than collapses, is abnormal. The large arteries of the neck and limbs and the aorta should be evaluated for bruits.
If the diagnosis is suspected, ESR, C-reactive protein, and CBC are determined. In most patients, ESR and C-reactive protein are elevated; anemia of chronic disease is common. Occasionally, platelets are elevated, and serum albumin and total protein, if measured, are low. Mild leukocytosis is commonly detected but is nonspecific.
If the diagnosis is suspected, biopsy of an artery is recommended. Because inflamed segments often alternate with normal segments, a segment that appears abnormal should be sampled if possible. Usually, the temporal artery is biopsied from the side that is symptomatic, but the occipital artery can also be biopsied if it appears abnormal. The optimal length of temporal artery to remove is unclear, but longer samples, up to 5 cm, increase the yield. The added diagnostic value of bilateral temporal artery biopsy is small. Treatment should not be delayed to do the biopsy. Biopsy can be done up to 2 wk or perhaps more after treatment is started because the inflammatory infiltrate is slow to resolve.
If patients have pulse deficits, the aorta and its branches are imaged (see see Imaging Tests Used in Takayasu Arteritis).
Treatment should be started as soon as giant cell arteritis is suspected, even if biopsy is going to be delayed for several days.
Corticosteroids are the cornerstone of treatment. Corticosteroids rapidly reduce symptoms and prevent vision loss in most patients. The optimal initial dose, tapering schedule, and total length of treatment are debated. For most patients, an initial dose of prednisone 40 to 60 mg po once/day (or equivalent) for 4 wk, followed by gradual tapering, is effective. If patients have visual disturbances, an initial dose of IV methylprednisolone 500 to 1000 mg once/day for 3 to 5 days can be tried in an attempt to help prevent further decline in vision, particularly in the contralateral eye. Saving vision probably depends more on how rapidly corticosteroids are started than their dose. Optic nerve infarction, once started, cannot be reversed regardless of corticosteroid dose.
If symptoms lessen, prednisone can be tapered gradually from doses of up to 60 mg/day based on the patient's response, usually as follows: by 5 to 10 mg/day every week to 40 mg/day, by 2 to 5 mg/day every week to 10 to 20 mg/day, then by 1 mg/day every month thereafter until the drug is stopped. ESR alone should not be used to evaluate patient response (and disease activity). Clinical symptoms must also be used. C-reactive protein can sometimes be more useful than ESR if ESR is elevated because many elderly patients have an elevated ESR due to elevated fibrinogen levels or undiagnosed monoclonal gammopathies.
Most patients require at least 2 yr of treatment with corticosteroids. Long-term use of corticosteroids can have significant adverse effects and thus should be limited if possible. More than one half of patients taking these drugs have drug-related complications. Consequently, alternative therapies are being studied. If patients cannot tolerate corticosteroids or if symptoms return when the dose is tapered, methotrexate 0.3 mg/kg/wk may be useful. In some patients, methotrexate can have a corticosteroid sparing effect and reduce flare-ups. Elderly patients taking prednisone long term should be given a bisphosphonate to prevent osteoporosis.
TNF inhibitors have not been shown to be effective.
Low-dose aspirin (81 to 100 mg po once/day) may help prevent ischemic events and should be prescribed for all patients unless contraindicated.
Last full review/revision April 2013 by Carmen E. Gota, MD
Content last modified May 2013