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Giant Cell Arthritis or Temporal Arthritis and Polymialgia Romatic


• It is the most common primary vasculitis.

• It is a granulomatous vasculitis involving large vessels.

• It is usually seen over 50 years old and in women.

• It often involves the carotid artery and its branches (most commonly the temporal artery).

• DHA; It occurs with head/scalp pain, jaw claudication, fever, increased erythrocyte sedimentation rate.

• The most feared complication is ophthalmic artery involvement (may result in irreversible vision loss).

• Cerebrovascular events (vertigo, transient ischemic attack, stroke, etc.) and signs of large vessel involvement (claudication in the extremities, blood pressure-pulse difference, etc.) can be seen.

• Polymyalgia may accompany rheumatica.

Diagnosis

• Clinical findings and temporal artery biopsy are combined in diagnosis.

• In case of suspected DHA accompanied by visual impairment, biopsy is not expected for diagnosis.

Steroids should be given immediately (biopsy can be taken up to 14 days after starting steroids).

• Detection of hypoechoic halo around the artery in Doppler USG is 100% specific.

Treatment

• The main treatment is steroids.

• Tocilizumab (anti IL6 receptor antibody) is more effective than steroid therapy.

• In the presence of vision-threatening involvement, pulse steroid should be given.

Polymialgia Romatic

• It is the most common disease accompanying DHA.

• It is usually seen over 50 years old and in women.

• It is characterized by proximal muscle pain.

• No loss of muscle strength.

• Sedimentation rate and CRP are significantly higher.

• Muscle enzymes, EMG and muscle biopsy are normal.

• It responds dramatically to low-dose steroids (10-20 mg/day).

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