Beyond Giant Cell Arteritis and Takayasu's Arteritis: Secondary Large Vessel Vasculitis and Vasculitis Mimickers
Alvise Berti1,2, Marta Casal Moura3, Elia Sechi4
1Rheumatology Department, Santa Chiara Regional Hospital and Department of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Largo Madaglie D'Oro 9, 38121, Trento, Italy. alvise.berti@apss.tn.it.
Insights
Diagnosing large vessel vasculitis (LVV) can be challenging. This review outlines conditions mimicking systemic, vascular, or cranial symptoms of giant cell arteritis and Takayasu arteritis.
Area of Science:
- Rheumatology
- Internal Medicine
- Vascular Medicine
Background:
- Large vessel vasculitis (LVV), including giant cell arteritis (GCA) and Takayasu arteritis (TAK), presents diagnostic challenges.
- Mimicking conditions can obscure the diagnosis, particularly with atypical or incomplete presentations.
Purpose of the Study:
- To review the differential diagnoses of LVV based on primary clinical manifestations.
- To categorize mimickers by systemic, vascular, and cranial presentations.
Main Methods:
- Literature review of conditions mimicking LVV.
- Categorization of differential diagnoses according to clinical presentation.
Main Results:
- Systemic symptoms (fever, weight loss, elevated inflammatory markers) can mimic neoplastic, infectious, or other inflammatory diseases.
- Vascular manifestations (ischemia, stenosis, aneurysms) require exclusion of atherosclerosis and non-inflammatory vascular conditions.
- Cranial symptoms (headache, vision loss, jaw claudication) necessitate consideration of cerebrovascular, neurological, and ophthalmologic disorders.
Conclusions:
- Accurate diagnosis of LVV requires careful consideration of mimickers across systemic, vascular, and cranial domains.
- A multidisciplinary approach is recommended for challenging and atypical LVV cases.
Purpose Of Review:
To provide an overview of mimickers of large vessel vasculitis (LVV), by the main presenting manifestation, i.e., systemic, vascular, and cranial manifestations.
Recent Findings:
The main differential diagnoses in patients with giant cell arteritis (GCA) and Takayasu arteritis (TAK) presenting with systemic manifestations (i.e., fever, anorexia, weight loss, night sweats, arthralgia/myalgia, and/or increased inflammatory indexes) are neoplastic, infectious, or other inflammatory conditions. In patients with vascular manifestations (such as peripheral ischemia, vascular stenoses, or aneurysms), atherosclerosis and non-inflammatory vascular diseases should be excluded. In those presenting with predominant cranial symptoms (i.e., temporal headache, jaw claudication, scalp tenderness, transient or permanent vision loss), other causes of headache, cerebrovascular accidents, optic neuropathy, and neuromuscular syndromes need to be considered. The diagnosis of LVV maybe challenging, especially when patients present with atypical or incomplete clinical forms. In these cases, a multidisciplinary approach is strongly recommended.
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