GIANT CELL (TEMPORAL) ARTERITIS - 11/09/11
Résumé |
Giant cell (temporal) arteritis (GCA) is a well-recognized cause of headache, polymyalgia rheumatica (PMR), inflamed superficial temporal arteries, and jaw claudication in an elderly patient with a high erythrocyte sedimentation rate (ESR). The diagnosis can be confirmed by temporal artery biopsy (TAB), and treatment with oral corticosteroids usually relieve symptoms and prevent vasculitic complications.
Yet GCA can pose difficult diagnostic and therapeutic problems. Diagnostically, many symptoms that are typical of GCA are nonspecific. Headache, the most common symptom in patients with GCA12 and the most frequent reason patients seek neurologic consultation,35 can accompany innumerable other diseases. There are no specific noninvasive tests for GCA. The ESR is increased in 97% of patients with GCA,12 so a normal ESR may bring the diagnosis into question, but only a TAB offers confirmatory evidence for GCA.28, 29 In one large series12 a third of TABs performed over a 3-year period showed vasculitis. Many physicians are reluctant to perform an invasive test with a 67% chance of a negative result. Some patients have unusual manifestations that are nonspecific for GCA, including stroke which is also endemic in the elderly. It can be difficult, impossible, or erroneous in any one patient to ascribe GCA as the one and only cause of stroke in a particular patient. Many clinicians assume that GCA does not lead to neurologic problems other than certain well-recognized neuro-ophthalmologic disorders. As usual, a middle ground is needed based on an appreciation of the neurologic complications that are caused by GCA and its treatment, and other comorbid illnesses.
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Vol 15 - N° 4
P. 893-902 - novembre 1997 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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