# Bilateral optic perineuritis: a rare manifestation of giant cell arteritis - case report and literature review

**Authors:** Jnadi Madkhali, Ahmed B. Aba Alkhail, Mohammed A. Aldriweesh, Yaser Al Malik

PMC · DOI: 10.3389/fopht.2025.1598302 · Frontiers in Ophthalmology · 2025-07-04

## TL;DR

This paper reports a rare case of optic perineuritis caused by giant cell arteritis and emphasizes the importance of early diagnosis and treatment to prevent vision loss.

## Contribution

The paper presents a rare case linking bilateral optic perineuritis to giant cell arteritis and underscores the need for prompt diagnosis and treatment.

## Key findings

- A 75-year-old patient with bilateral optic perineuritis was diagnosed with giant cell arteritis via temporal artery biopsy.
- Treatment with high-dose steroids and tocilizumab improved symptoms and stabilized vision.
- Early diagnosis and aggressive treatment are critical to prevent irreversible vision loss in GCA-associated OPN.

## Abstract

Giant cell arteritis (GCA) is a granulomatous vasculitis in older individuals that primarily affects medium-to-large vessels. Owing to the involvement of the ophthalmic arteries, GCA can lead to severe ischemic complications, including vision loss. Optic perineuritis (OPN) is characterized by inflammation around the optic nerve sheath and is a rare manifestation of GCA with diagnostic and therapeutic challenges.

This case study reports a 75-year-old female presenting with subacute constitutional symptoms of fever and poor appetite with bilateral eye pain and visual disturbance. The patient had elevated inflammatory markers, specifically an erythrocyte sedimentation rate of 120 mm/h, with imaging findings consistent with bilateral OPN and temporal artery biopsy-proven GCA. Treatment with high-dose dexamethasone, followed by oral prednisolone and tocilizumab, led to symptomatic improvement in vision stabilization.

This case highlights the importance of recognizing OPN as a possible manifestation of GCA. Although cases of OPN are mostly idiopathic, it can rarely represent the first manifestation of GCA. Therefore, prompt diagnosis through brain imaging and temporal artery biopsy is essential, and aggressive treatment with steroids is crucial for managing GCA-associated OPN to prevent irreversible vision loss.

## Linked entities

- **Chemicals:** dexamethasone (PubChem CID 5743), prednisolone (PubChem CID 5755)
- **Diseases:** giant cell arteritis (MONDO:0008538), optic perineuritis (MONDO:0044690)

## Full-text entities

- **Diseases:** eye pain (MESH:D058447), inflammation (MESH:D007249), fever (MESH:D005334), granulomatous vasculitis (MESH:D015267), GCA (MESH:D013700), OPN (MESH:D052958), ischemic (MESH:D002545), vision loss (MESH:D014786)
- **Chemicals:** prednisolone (MESH:D011239), tocilizumab (MESH:C502936), dexamethasone (MESH:D003907), steroids (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12270863/full.md

## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12270863/full.md

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Source: https://tomesphere.com/paper/PMC12270863