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.
Abstract

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