This reviews clinical
presentation, diagnosis and management.
Giant cell arteritis can affect many arteries throughout the body, producing symptoms
and signs which mimic many other medical and surgical conditions:
Systemic symptomsflu like with fever.
Myalgic symptoms.
Arteritislocal inflammation, partial or complete occlusion.
Temporal arteritis a clinical syndrome due to giant cell arteritis localized to the
region of the temporal artery.
Polymyalgia rheumatica is due to giant cell arteritis and causes a clinical syndrome of
proximal, symmetrical extremity pain and stiffness.
Both B and C are diseases of elderly people. They may coexist or appear separately.
Diagnosis is largely by clinical history, a substantially raised sed rate, exclusion of
other conditions and confirmatory biopsy evidence.
Sudden painless loss of vision in one eye due to arterial occlusion is a dreaded
complication of arteritis.
"Temporal artery biopsy samples are positive in 60-80% of patients with giant cell
arteritis, but in only 15-20% of patients with polymyalgia rheumatica, in whom biopsy for
polymyalgia alone is not justified."
Corticosteroids are essential for the treatment of polymyalgia rheumatica and temporal
arteritis. They rapidly relieve the incapacitating symptoms and reduce the incidence of
blindness. Response to steroids is dramatic.
The need for long-term steroid therapy causes concern. Titrating a gradual reduction in
dose guided by the clinical picture and the sed rate is reasonable. Most studies indicate
that between 1/3 and 1/2 of patients can stop steroids after 2 years. The risk of relapse
must be balanced against steroid related side effects.
"Polymyalgia rheumatica and temporal arteritis are among the most rewarding diseases
for a clinician to diagnose and treat because the unpleasant symptoms and serious
consequences can be rapidly prevented with corticosteroids.
BMJ May 3, 1997; 312: 1329-32 Clinical review from Notingham City Hospital, UK
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