# A Delayed Acute Vestibular Syndrome and Diplopia in Ramsay Hunt Syndrome With Absent Facial Nerve Paralysis After Partially Treated Varicella-Zoster Virus (VZV) Oticus

**Authors:** Ambuj Bhalla, Zeeshan Zubair, Lisle W Blackbourn, Jorge Kattah

PMC · DOI: 10.7759/cureus.99653 · 2025-12-19

## TL;DR

An 82-year-old man with Ramsay Hunt syndrome showed delayed vestibular symptoms and diplopia without facial paralysis, responding well to antiviral and steroid treatment.

## Contribution

This case highlights an atypical Ramsay Hunt syndrome presentation with vestibular symptoms and absent facial palsy.

## Key findings

- MRI showed enhancement of cranial nerves VII and VIII without clinical facial motor deficit.
- Antiviral and corticosteroid therapy resolved diplopia and nystagmus within a week.
- Gait improved significantly within four weeks, preventing long-term complications.

## Abstract

Ramsay Hunt syndrome (herpes zoster oticus) is an uncommon neurological complication of varicella-zoster virus (VZV) reactivation caused by inflammation of the geniculate ganglion of cranial nerve VII. While Ramsay Hunt syndrome classically affects cranial nerve VII, concomitant involvement of cranial nerve VIII is well described. The classic triad includes unilateral lower motor neuron facial paralysis, otalgia, and vesicular rash in the auricle or auditory canal. Atypical presentations without these features are recognized and may delay diagnosis.

We report an 82-year-old man with recent herpes zoster oticus who developed acute vestibular syndrome with gait instability, left-beating nystagmus, and vertical diplopia. He had left ear and temporal pain but no facial weakness. Contrast-enhanced MRI showed enhancement of cranial nerves VII and VIII in the cerebellopontine angle without clinical facial motor deficit.

Following sequential antiviral therapy (intravenous acyclovir followed by oral valacyclovir) and corticosteroids, diplopia and nystagmus resolved within one week with substantial gait improvement by four weeks.

This case highlights Ramsay Hunt syndrome presenting with predominant vestibulocochlear dysfunction despite radiographic facial nerve involvement. Prompt antiviral and corticosteroid therapy can prevent permanent sequelae such as sensorineural hearing loss or neurotrophic keratitis. Clinicians should maintain a high index of suspicion for VZV-related cranial polyneuropathy in older adults with acute vestibular syndrome after recent zoster, even in the complete absence of facial palsy.

## Linked entities

- **Chemicals:** acyclovir (PubChem CID 135398513), valacyclovir (PubChem CID 135398742)
- **Diseases:** Ramsay Hunt syndrome (MONDO:0005769), sensorineural hearing loss (MONDO:0010576), neurotrophic keratitis (MONDO:0015290)

## Full-text entities

- **Diseases:** Diplopia (MESH:D004172), Ramsay Hunt Syndrome (MESH:D016697), Acute Vestibular Syndrome (MESH:D020338), vesicular rash (MESH:D005076), sensorineural hearing loss (MESH:D006319), facial motor deficit (MESH:D005155), Paralysis (MESH:D010243), left-beating nystagmus (MESH:D009759), vestibulocochlear dysfunction (MESH:C536346), otalgia (MESH:D004433), neurotrophic keratitis (MESH:D007634), facial weakness (MESH:D018908), polyneuropathy (MESH:D011115), neurological complication (MESH:D002493), facial palsy (MESH:D005158), zoster (MESH:D006562), temporal pain (MESH:D010146), gait instability (MESH:D043171)
- **Chemicals:** acyclovir (MESH:D000212), valacyclovir (MESH:D000077483)
- **Species:** Human alphaherpesvirus 3 (Varicella-zoster virus, no rank) [taxon 10335]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12813963/full.md

---
Source: https://tomesphere.com/paper/PMC12813963