# Beyond the Usual Suspects: Unilateral Optic Disc Edema as a Rare Initial Sign of Vogt-Koyanagi-Harada Syndrome

**Authors:** Vipin Rana, Vikas Sharma, Kanwaljeet Singh, Amit Nandan Tripathi, Ranjit Goenka, Ashish Markan

PMC · DOI: 10.22336/rjo.2025.44 · 2025-04-01

## TL;DR

A rare case of Vogt-Koyanagi-Harada syndrome initially presented with optic disc edema, highlighting the need for early diagnosis using imaging and spinal fluid analysis.

## Contribution

This paper presents a rare initial presentation of VKH syndrome with unilateral optic disc edema and emphasizes the role of advanced imaging and cerebrospinal fluid analysis in diagnosis.

## Key findings

- Unilateral optic disc edema can be an initial sign of VKH syndrome.
- Multimodal imaging and cerebrospinal fluid analysis are critical for early diagnosis of VKH.
- Prompt treatment with corticosteroids and azathioprine can prevent chronic disease progression.

## Abstract

To report a case of unilateral optic disc edema as a rare initial presentation of Vogt-Koyanagi-Harada (VKH) syndrome and emphasize the importance of early diagnosis using advanced imaging and cerebrospinal fluid analysis.

We present the case of a 23-year-old male who initially presented with unilateral optic disc edema, retro-orbital pain, and headache, progressing to bilateral involvement with serous retinal detachments. Advanced imaging, including fundus fluorescein angiography (FFA), Indocyanine green angiography (ICG), and Enhanced depth imaging-Optical coherence tomography (EDI-OCT), revealed hallmark findings of VKH, such as choroidal granulomas and increased choroidal thickness. Cerebrospinal fluid analysis confirmed pleocytosis and melanin-laden macrophages, which helped to establish the diagnosis. The patient was treated with high-dose intravenous corticosteroids and azathioprine, with significant improvement.

VKH progresses through prodromal, acute uveitic, chronic, and recurrent phases. Although typically presenting with panuveitis, isolated optic disc edema as an initial sign is rare. Early diagnosis requires multimodal imaging and cerebrospinal fluid analysis to differentiate VKH from other inflammatory and infectious aetiologies.

This case highlights the importance of considering VKH in patients presenting with disc edema, whether unilateral or bilateral, particularly when accompanied by vitreous cells. Advanced ocular imaging and thorough systemic evaluation are critical for early diagnosis. Prompt treatment can prevent progression to chronic disease and irreversible vision loss.

## Linked entities

- **Chemicals:** azathioprine (PubChem CID 2265)
- **Diseases:** Vogt-Koyanagi-Harada syndrome (MONDO:0018092), panuveitis (MONDO:0017255)

## Full-text entities

- **Diseases:** choroidal granulomas (MESH:D006099), serous retinal detachments (MESH:D012163), pleocytosis (MESH:D007964), Vogt-Koyanagi-Harada (VKH) syndrome (MESH:D014607), orbital pain (MESH:D010146), vision loss (MESH:D014786), Optic Disc Edema (MESH:D010211), headache (MESH:D006261), inflammatory (MESH:D007249), panuveitis (MESH:D015864)
- **Chemicals:** melanin (MESH:D008543), azathioprine (MESH:D001379), fluorescein (MESH:D019793), Indocyanine green (MESH:D007208)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12277989/full.md

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Source: https://tomesphere.com/paper/PMC12277989