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An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
What is the best approach to diagnosing large-vessel vasculitis?
Wolfgang A Schmidt1, Erika Gromnica-Ihle
1Medical Centre for Rheumatology Berlin-Buch, Karower Strasse 11, 13125 Berlin, Germany. w.schmidt@immanuel.de
Insights
Large-vessel vasculitides like temporal arteritis and Takayasu's arteritis affect major arteries. Diagnosis involves clinical exams and advanced imaging like ultrasonography and angiography for effective treatment.
Area of Science:
- Vascular Medicine
- Rheumatology
- Diagnostic Imaging
Background:
- Temporal arteritis (TA) and Takayasu's arteritis (TAK) are primary large-vessel vasculitides.
- TA presents with headache, visual impairment, and polymyalgia rheumatica symptoms.
- TAK often manifests with systemic symptoms like fever, fatigue, and arthralgia.
Purpose of the Study:
- To review diagnostic methods for TA and TAK.
- To highlight clinical and imaging findings in large-vessel vasculitides.
- To compare conventional and novel imaging techniques.
Main Methods:
- Clinical examination including palpation, auscultation, and fundoscopy.
- Duplex ultrasonography for temporal and axillary arteries.
- Advanced imaging: angiography, MRI, CT, and PET.
Main Results:
- Clinical signs like jaw claudication and temporal artery abnormalities suggest TA.
- Ultrasonography reveals characteristic wall swelling, stenosis, and occlusions.
- Imaging methods show distinct aortic and branch artery changes in TA and TAK.
Conclusions:
- Early diagnosis of TA and TAK relies on integrating clinical findings and imaging.
- Ultrasonography is valuable for TA and large-vessel giant cell arteritis.
- Advanced imaging offers less invasive alternatives to angiography for detecting inflammatory changes.
Abstract:
Temporal arteritis, including large-vessel giant cell arteritis, and Takayasu's arteritis are the two primary large-vessel vasculitides. Patients with temporal arteritis often present with headache, swollen temporal arteries, impairment of vision or symptoms of polymyalgia rheumatica. Clinical examination includes palpation of the temporal arteries and radial pulses, auscultation of the subclavian and axillary region, and fundoscopy. The presence of jaw claudication, diplopia and temporal artery abnormalities correlates with a high probability of positive histology. Duplex ultrasonography of the temporal arteries delineates a characteristic hypoechoic, oedematous wall swelling, stenoses and occlusions. It detects the same pathologies in the axillary arteries and other arteries in large-vessel giant cell arteritis. Angiography, magnetic resonance imaging, magnetic resonance angiography, electron beam computed tomography, computed tomography angiography and positron emission tomography show characteristic changes in the aorta and its primary branches in large-vessel giant cell arteritis and Takayasu's arteritis. Takayasu's arteritis often begins with diffuse symptoms such as low-grade fever, arthralgia, fatigue and weight loss. Clinical examination is important to detect bruits, pulse reduction and blood pressure differences. Profound experience exists with angiography. Other imaging methods are interesting alternatives as they are less invasive and may depict the inflammatory wall swelling.
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