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Published on: February 8, 2019
Takayasu arteritis of subclavian artery in a Caucasian
Insights
Takayasu arteritis, a rare inflammatory artery disease, can affect young women worldwide. This case highlights its presentation in a Caucasian woman with subclavian artery stenosis.
Area of Science:
- Cardiology
- Rheumatology
- Immunology
Background:
- Takayasu arteritis is an inflammatory, obliterative disease of medium and large arteries, often affecting the aorta and its branches.
- It is classified as a giant cell arteritis and can present with systemic symptoms mimicking other conditions.
- While historically associated with specific demographics, it is now recognized globally.
Observation:
- A Caucasian woman presented with nonspecific symptoms including fatigue and upper back pain.
- Physical examination revealed an absent left radial pulse and a significant blood pressure differential.
- Radiological imaging confirmed left subclavian artery stenosis.
Findings:
- The patient's presentation and imaging findings were consistent with Takayasu arteritis.
- This case underscores that Takayasu arteritis affects diverse populations, not limited by ethnicity or origin.
- Early diagnosis relies on clinical suspicion, physical findings, and advanced imaging.
Implications:
- Prompt diagnosis and management are crucial to prevent severe vascular complications.
- This case contributes to the understanding of Takayasu arteritis presentation in non-traditional demographics.
- Further research into the autoimmune etiology may reveal novel therapeutic targets.
Abstract:
Takayasu arteritis, an inflammatory and obliterative disease of medium and large arteries, is classified as a giant cell arteritis. It has a predilection for the aortic arch, its main branches, and coronary and pulmonary arteries. The early symptoms of Takayasu arteritis may be mainly systemic and may resemble polymyalgia rheumatica. The etiology is unknown but autoimmunity has been suggested to play a role. Diagnosis is based on symptoms, physical findings, and imaging, because tissue diagnosis is rarely feasible. Unlike atherosclerotic vascular disease, Takayasu arteritis affects primarily, but not exclusively, young women. Contrary to earlier reports, it is not limited to the women of Japanese origin but is present worldwide. The current report is of a Caucasian woman who presented with nonspecific complaints of upper back pain, weakness, malaise, and fatigue. Her physical examination revealed absent left radial pulse and a blood pressure differential, later confirmed by radiological imaging studies to be due to left subclavian artery stenosis consistent with Takayasu arteritis. The presentation and management of the patient is described, and Takayasu arteritis is succinctly reviewed.
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