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Giant cell arteritis (GCA), also called temporal arteritis, is an inflammatory autoimmune disease of large blood vessels. [ 4 ] [ 7 ] Symptoms may include headache , pain over the temples, flu-like symptoms , double vision , and difficulty opening the mouth. [ 3 ]
Giant cell arteritis: Large and medium arteries, can affect coronary arteries None specific Confirmed 200 per 100,000 (over age 50) [32] [33] Takayasu's arteritis: Large arteries, including the aorta: None specific Confirmed Rare, more common in East Asia [33] [34] Behçet's disease: Small to large vessels in mouth, genitals, eyes, skin None ...
An overall feeling of illness or flu-like symptoms. Low-grade (mild) fever [12] or abnormal temperature is sometimes present. High or spiking fevers may occur in patients who also have giant cell arteritis. [2] Generalized weakness Note that this is generalized weakness, not muscle weakness. The presence of muscle weakness likely indicates a ...
The disease's symptoms can range from catastrophic neurological impairment to an asymptomatic condition brought on by impalpable pulses or bruits. [7] Non-specific features include mild anemia, myalgia, arthralgia, weight loss, malaise, night sweats, and fever. [8] Giant cell arteritis (GCA) is the most common type of systemic vasculitis in adults.
Arteritis is a vascular disorder characterized by inflammation of the walls of arteries, [1] usually as a result of infection or autoimmune responses. Arteritis, a complex disorder, is still not entirely understood. [2] Arteritis may be distinguished by its different types, based on the organ systems affected by the disease. [2]
Sudden visual loss is the most common symptom in AAION, [1] and is most often accompanied by other symptoms of temporal arteritis: such as jaw claudication, scalp tenderness, unintentional weight loss, fatigue, myalgias and loss of appetite. [1] A related disease called polymyalgia rheumatica has a 15 percent incidence of giant cell arteritis.
The revised five-factor score is associated with five-year mortality from GPA and is based on these criteria: Age greater than 65 years, cardiac symptoms, gastrointestinal involvement, chronic kidney disease, and the absence of ear, nose, and throat symptoms. [7] With corticosteroids and cyclophosphamide, five-year survival is over 80%. [13]
Main symptoms Primary large vessel vasculitis [8] Takayasu arteritis: Diminished or absent pulses, vascular bruits, hypertension, Takayasu retinopathy, and aortic regurgitation. [9] Giant cell arteritis: Headache, scalp tenderness, jaw claudication, and blindness. [10] Primary medium vessel vasculitis [8] Polyarteritis nodosa