Takayasu arteritis Flashcards
What vessels are affected with Takayasu arteritis?
Takayasu arteritis is a granulomatous vasculitis of large arteries, primarily affecting the aortic arch and its branches, leading to stenosis, aneurysm formation, occlusion, or coarctation.
What histopathological findings are seen in Takayasu arteritis?
Characteristic histopathologic findings include mononuclear infiltrates and granulomatous inflammation of the vascular media, leading to arterial wall thickening and occlusion. Granulomatous inflammation of the vascular media, with mononuclear infiltrates, transmural fibrosis, and narrowing of the arterial lumen.
Which population is most commonly affected by Takayasu arteritis?
Young adults aged 20-40 years, particularly Asian females.
What are the primary risk factors for Takayasu arteritis?
Young age (20-40 years), female gender, and Asian ethnicity.
What are the constitutional symptoms of Takayasu arteritis?
Fever, weight loss, fatigue, and myalgias.
What are the dermatological manifestations of Takayasu arteritis?
- Livedo reticularis
- Tender nodules
- Purpura
What CNS manifestations are seen with Takayasu arteritis?
vision loss, neurological deficits, stroke.
What are the arterial-occlusive symptoms of Takayasu arteritis?
- Claudication
- pulse deficits (carotid, radial, ulnar)
- blood pressure discrepancies between limbs
- tenderness and audible bruits over affected vessels
- Renal artery involvement (higher in Asian populations) overall ranges from 11.5% to 62%
What vessel is primarily implicated in Takayasu arteritis?
The aorta.
What deadly complications can arise from Takayasu arteritis?
Aortic aneurysms, aortic regurgitation, coarctation, myocardial infarction, stroke.
What imaging modality is used to diagnose Takayasu arteritis?
Magnetic resonance angiography (MRA) or computed tomography angiography (CTA) is used to visualize vessel narrowing, aneurysms, or coarctation. Arterial narrowing in TA can manifest as audible bruits, blood pressure discrepancies, pulse deficits, and distal ulcerations.
What laboratory findings are commonly seen in Takayasu arteritis?
Elevated inflammatory markers such as erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP).
What is the first-line treatment for Takayasu arteritis?
Corticosteroids to control inflammation.
What other treatments are used for refractory Takayasu arteritis?
Immunosuppressive agents such as methotrexate, azathioprine, mycophenolate mofetil, or tocilizumab.
What intervention may be required for severe arterial stenosis or coarctation in Takayasu arteritis?
Angioplasty or stenting.