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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
Bilateral vertebral artery occlusion with retrograde basilary flow in three cases of giant cell arteritis
Markus Boettinger1, Markus Robert Boettinger, Schreglmann Sebastian
1University of Regensburg, Neurology, Universitaetsstr 84, Regensburg, 93053, Germany.
Insights
Giant cell arteritis (GCA) can cause rare, life-threatening vertebrobasilar ischaemia. This study highlights three cases of bilateral vertebral artery occlusion, emphasizing the need for early diagnosis and management of GCA-related vascular complications.
Area of Science:
- Neurology
- Vascular Medicine
- Rheumatology
Background:
- Giant cell arteritis (GCA) is an inflammatory condition that can affect large arteries, including the vertebral arteries.
- Vertebrobasilar ischaemia is a rare but severe complication of GCA, potentially leading to devastating neurological deficits.
- Bilateral vertebral artery occlusion presents a unique challenge in managing GCA patients.
Purpose of the Study:
- To describe the clinical presentation, diagnostic findings, and outcomes of three patients with giant cell arteritis and bilateral vertebral artery occlusion.
- To investigate the role of neurovascular imaging in identifying vertebrobasilar compromise in GCA.
- To discuss potential management strategies and prognostic factors for patients with this rare complication.
Main Methods:
- Case series reporting on three patients diagnosed with GCA and bilateral vertebral artery occlusion.
- Utilized advanced neurovascular imaging techniques including CT-angiography, MR-angiography, and colour-coded duplex sonography.
- Monitored patients' clinical status, neurological outcomes, and response to treatment over a 12-month follow-up period.
Main Results:
- All three patients exhibited inflammation of the vertebral vessel wall and flow reversal in the basilar artery.
- One patient experienced a fatal massive brainstem infarction.
- The two surviving patients remained stroke-free at 12 months on warfarin and steroid therapy, despite persistent bilateral vertebral artery occlusion and retrograde basilar artery flow.
Conclusions:
- Bilateral vertebral artery occlusion in GCA is a high-risk condition associated with significant morbidity and mortality.
- Effective management likely depends on potent immunosuppression, addressing comorbid atherosclerotic disease, and developing adequate collateral circulation.
- Identifying patients at risk for vertebrobasilar ischaemia is crucial for selecting adjunctive treatments, such as anticoagulation, in GCA management.
Abstract:
Vertebrobasilar ischaemia is a rare life-threatening complication in giant cell arteritis (GCA). We report three patients with bilateral vertebral artery occlusion. Neurovascular imaging, including CT-angiography, MR-angiography and colour-coded duplex sonography revealed flow reversal in the basilar artery as well as inflammation of the vertebral vessel wall. The first patient died from massive brainstem infarction, the other two patients survived the initial inflammatory phase of GCA. No stroke recurrence at 12 months' follow-up on warfarin and steroid treatment was observed. Bilateral distal vertebral artery occlusion and retrograde basilar artery flow persisted.Outcome in these patients is dependant on potent immunosuppression, concurrent atherosclerotic steno-occlusive disease and presence and/or rapid development of sufficient collateral pathways into the vertebrobasilar circulation. The identification of patients with high risk of ischaemia due to compromised vertebrobasilar flow may be important to select adjunct treatment to immunosuppression, such as anticoagulation in GCA.
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