# Large Sporadic Vestibular Schwannoma Causing Brainstem Compression and Obstructive Hydrocephalus in a Young Adult

**Authors:** Adebola O Adetiloye, Anim Asif, Olurotimi J Badero

PMC · DOI: 10.7759/cureus.104905 · Cureus · 2026-03-09

## TL;DR

A 21-year-old man had a large sporadic vestibular schwannoma causing brainstem compression and hydrocephalus, emphasizing the need for early imaging in young patients with audiovestibular symptoms.

## Contribution

The case presents a rare instance of a large sporadic vestibular schwannoma in a young adult with a somatic NF2 mutation.

## Key findings

- A 21-year-old man had a large vestibular schwannoma causing brainstem compression and obstructive hydrocephalus.
- Tumor analysis revealed a somatic mutation in NF2, supporting a diagnosis of sporadic vestibular schwannoma.
- The case underscores the importance of early neuroimaging in young patients with progressive audiovestibular symptoms.

## Abstract

Sporadic vestibular schwannomas are typically slow-growing, unilateral cerebellopontine angle benign tumors that occur in middle-aged and older adults and rarely present in individuals younger than 30 years. We describe the case of a 21-year-old man who presented with progressive unilateral hearing loss and tinnitus and was found to have a large vestibular schwannoma causing brainstem compression and obstructive hydrocephalus. Tumor analysis demonstrated a somatic mutation in neurofibromatosis type 2 (NF2), confined to the tumor, supporting a diagnosis of sporadic vestibular schwannoma in the absence of NF2 features. This case highlights the importance of early neuroimaging in patients with persistent or progressive unilateral audiovestibular symptoms.

## Linked entities

- **Genes:** NF2 (NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor) [NCBI Gene 4771]
- **Diseases:** vestibular schwannoma (MONDO:0001569), neurofibromatosis type 2 (MONDO:0007039), obstructive hydrocephalus (MONDO:0001896)

## Full-text entities

- **Genes:** NF2 (NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor) [NCBI Gene 4771] {aka ACN, BANF, SCH, SWNV, merlin-1}
- **Diseases:** drop metastasis (MESH:D009362), numbness (MESH:D006987), increased intracranial pressure (MESH:D019586), Hydrocephalus (MESH:D006849), diminished right-sided hearing (MESH:D000069584), brain or spinal tumors (MESH:D001932), spinal neurofibromas (MESH:D009455), optic disc edema (MESH:D010211), headaches (MESH:D006261), Compression (MESH:D009408), blurred vision (MESH:D014786), Tumor (MESH:D009369), tinnitus (MESH:D014012), Schwannoma (MESH:D009442), nausea (MESH:D009325), schwannomatosis (MESH:C536641), gait disturbance (MESH:D020233), leptomeningeal disease (MESH:D008577), vertigo (MESH:D014717), Sporadic vestibular schwannomas (MESH:D009464), hearing loss (MESH:D034381), sensorineural hearing loss (MESH:D006319)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** c.586C>T, p.Arg196*

## Full text

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## Figures

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## References

13 references — full list in the complete paper: https://tomesphere.com/paper/PMC12970144/full.md

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Source: https://tomesphere.com/paper/PMC12970144