Giant cell arteritis: Difference between revisions
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==Background== |
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==Definition== |
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*[[Large-vessel vasculitis]] that occurs in older age and is associated with polymyalgia rheumatica |
*[[Large-vessel vasculitis]] that occurs in older age and is associated with polymyalgia rheumatica |
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==Epidemiology== |
=== Epidemiology === |
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*Most common systemic vasculitis in North America |
*Most common systemic vasculitis in North America |
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==Pathophysiology== |
=== Pathophysiology === |
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*Granulomatous inflammation of the aortic arch and extracranial carotid artery |
*Granulomatous inflammation of the aortic arch and extracranial carotid artery |
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==Clinical Manifestations== |
==Clinical Manifestations== |
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*Jaw claudication |
*Jaw claudication |
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*Visual loss |
*Visual loss |
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==Investigations== |
==Investigations== |
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***Negative: treat based on MD diagnosis (biopsy-negative GCA or other) |
***Negative: treat based on MD diagnosis (biopsy-negative GCA or other) |
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***Positive: treat as GCA |
***Positive: treat as GCA |
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==Management== |
==Management== |
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*Follow [[ESR]] for response |
*Follow [[ESR]] for response |
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*Annual chest x-rays for the first ten years, to monitor for thoracic aortic aneurysm |
*Annual chest x-rays for the first ten years, to monitor for thoracic aortic aneurysm |
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[[Category:Rheumatology]] |
[[Category:Rheumatology]] |
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Latest revision as of 18:32, 4 July 2025
Background
- Large-vessel vasculitis that occurs in older age and is associated with polymyalgia rheumatica
- Also known as temporal arteritis
Epidemiology
- Most common systemic vasculitis in North America
Pathophysiology
- Granulomatous inflammation of the aortic arch and extracranial carotid artery
Clinical Manifestations
- After 50 years
- Headache, usually unilateral with tenderness
- Polymyalgia rheumatica (PMR)
- Jaw claudication
- Visual loss
Prognosis
- Cycles of flares and remissions requiring adjustment in prednisone
- Very few can safely taper off of steroids altogether
Investigations
- Temporal artery biopsy
- Shows mononuclear cell infiltrate with granulomatous inflammation, and usually multinucleated giant cells
- Findings are still visible 6-12mo after starting therapy
- Ultrasound of temporal arteries
- Looking for "halo sign" of hypoechoic ring around Doppler flow
- Sn 55-100%, Sp 78-100% (more specific than sensitive)
- Disappears quickly with treatment
- MRI scalp arteries
McMaster Workup
- Initial investigation with ultrasound; if positive halo sign, can skip the rest
- Low or moderate
- Scalp artery MRI
- Normal: treat based on MD diagnosis
- Abnormal
- Temporal artery biopsy
- Negative: treat based on MD diagnosis (biopsy-negative GCA or other)
- Positive: treat as GCA
- Temporal artery biopsy
- Scalp artery MRI
- High
- Temporal artery biopsy
- Negative: treat based on MD diagnosis (biopsy-negative GCA or other)
- Positive: treat as GCA
- Temporal artery biopsy
ACR Classification Criteria
- Requires 3 of 5 criteria
- Age ≥50 years
- New localized headache
- Temporal artery tenderness or decreased temporal artery pulse
- ESR ≥ 50 mm/h: 10-20% false negative, though
- Artery biopsy consistent with GCA: Up to 40% false negative, related to skip lesions, small biopsies, or lack of temporal artery involvement
- Not diagnostic criteria
Management
- Prednisone 0.2-0.3mg/kg/day (and appropriate screening)
- Taper over 2 years, dropping by 5mg/d over a few weeks then slowing down
- Often aren't able to taper off altogether
- Low-dose ASA for cardiovascular and cerebrovascular protection
- Can consider adding steroid-sparing agent
- Tocilizumab (IL-6 receptor)
- Maybe methotrexate
- Not MMF or other DMARDs
- Follow ESR for response
- Annual chest x-rays for the first ten years, to monitor for thoracic aortic aneurysm