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Published on: February 8, 2019
Neuro-ophthalmic Manifestations of Giant Cell Arteritis: A Review
Jo-Ann Khoury1, Danah Albreiki1,2
1Department of Ophthalmology, University of Ottawa, Ottawa, Canada.
Insights
Giant cell arteritis (GCA) is a medical emergency causing vision loss. Early diagnosis of its varied neuro-ophthalmic signs is critical for prompt steroid treatment and preventing permanent damage.
Area of Science:
- Ophthalmology
- Rheumatology
- Neurology
Background:
- Giant cell arteritis (GCA) is the most common vasculitis in individuals over 50.
- It presents a medical emergency due to ischemic damage and risk of vision loss.
- Diagnosis can be challenging due to diverse clinical and neuro-ophthalmic manifestations.
Purpose of the Study:
- To review documented neuro-ophthalmic manifestations of GCA.
- To provide insight into rare presentations to improve diagnostic accuracy.
- To emphasize the importance of early intervention in suspected GCA cases.
Main Methods:
- Literature review of studies on GCA neuro-ophthalmic manifestations.
- Categorization of findings into afferent and efferent neuro-ophthalmic signs.
- Analysis of clinical presentations, diagnostic markers, and treatment strategies.
Main Results:
- Afferent manifestations include ischemic optic neuropathy, retinal/choroidal artery occlusion, ocular ischemic syndrome, and visual field loss.
- Efferent manifestations include cranial neuropathies (3rd, 4th, 6th nerves), extraocular muscle ischemia, and internuclear ophthalmoplegia.
- Rare presentations include tonic pupil, uveitis, and encephalopathy.
Conclusions:
- Suspected GCA requires systemic symptom inquiry, neuro-ophthalmic examination, inflammatory markers, and temporal artery biopsy (TAB).
- High clinical suspicion warrants immediate high-dose steroid initiation.
- Timely diagnosis and treatment are crucial to prevent irreversible vision loss.
Abstract:
Giant cell arteritis (GCA) is the most common vasculitis of large and medium vessels affecting adults over the age of 50. Due to its acute ischemic damage through a systemic inflammatory process, GCA is a medical emergency with the risk of permanent vision loss. Therefore, early intervention is critical. Patients often present with well-documented systemic manifestations such as jaw claudication, headache, scalp tenderness, and fatigue. These patients are usually subject to blood tests for inflammatory markers and temporal artery biopsy. However, clinical manifestations vary considerably and may masquerade as neuro-ophthalmic manifestations that are not pathognomonic of GCA. We conducted a review to discuss documented neuro-ophthalmic manifestations and provide insight into the rare presentations to help avoid pitfalls in its diagnosis. Findings from the included articles were sorted into afferent and efferent neuro-ophthalmic manifestations. According to our literature review, the main afferent manifestations documented are ischemic optic neuropathy, retinal artery occlusion, choroidal infarction, ocular ischemic syndrome, orbital inflammatory syndrome, and strokes causing visual field loss. The efferent manifestations include cranial neuropathy (3 , 4 , and 6 ), extraocular muscle ischemia, and internuclear ophthalmoplegia. Other rare causes are tonic pupil from ciliary ganglion involvement, uveitis, and encephalopathy. If GCA is suspected, in addition to inquiring about systemic symptoms and doing a complete neuro-ophthalmic exam, these patients should be sent for inflammatory serological markers, as well as temporal artery biopsy (TAB). If clinical suspicion remains high, high-dose steroids should be started immediately.
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