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Published on: February 8, 2019
Two cases of recurrent stroke in treated giant cell arteritis: diagnostic and therapeutic dilemmas
Alasdair J Fitzgerald1, James W Ironside, David M Summers
1Department of Rehabilitation Medicine, Astley Ainslie Hospital, Edinburgh, Scotland. alasdair.fitzgerald@nhs.net
Insights
Giant cell arteritis (GCA) patients face stroke risks from various causes. Even with treatment, persistent inflammation can lead to strokes, highlighting diagnostic challenges.
Area of Science:
- Neurology
- Rheumatology
- Vascular Medicine
Background:
- Giant cell arteritis (GCA) is associated with an increased risk of stroke.
- The precise cause of stroke in GCA patients remains unclear, complicating treatment decisions.
- Potential causes include atherosclerosis, ongoing arterial inflammation, or corticosteroid side effects.
Observation:
- Two GCA patients experienced recurrent strokes in different arterial territories after starting corticosteroid therapy.
- Cranial symptoms resolved and inflammatory markers normalized in these patients.
- Further investigation indicated persistent arteritis as the cause of the strokes.
Findings:
- Laboratory tests and imaging may not accurately reflect the cause of stroke in GCA patients.
- Persistent arteritis can cause strokes even when clinical and laboratory markers of inflammation appear controlled.
- Current diagnostic methods have limitations in assessing stroke etiology in GCA.
Implications:
- There is a critical need for improved methods to monitor GCA activity.
- Developing effective strategies to determine the optimal treatment for stroke prevention in GCA is essential.
- Further research is required to elucidate the pathophysiology of stroke in GCA and refine therapeutic approaches.
Abstract:
It is not established whether the increased risk of stroke in patients with giant cell arteritis (GCA) is because of atherosclerosis, persistent arterial inflammation, or an iatrogenic effect of corticosteroids. This creates difficulties in choosing the most appropriate treatment. We report 2 patients with GCA who developed repeated strokes involving different arterial territories following initiation of corticosteroid therapy, despite resolution of cranial symptoms and normalization of inflammatory markers. Subsequent investigation suggested persisting arteritis as the cause of these strokes. The cases revealed the limitations of laboratory tests or imaging techniques in determining the cause of stroke in recently diagnosed GCA. There is a need to develop effective means of monitoring GCA activity and to determine the most effective treatment approach in this circumstance.
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