Vestibular schwannoma (acoustic neuroma)
Benign Schwann-cell tumour of CN VIII at the cerebellopontine angle
Overview
A benign tumour of the vestibulocochlear nerve’s Schwann cells at the cerebellopontine angle. The classic presentation is UNILATERAL sensorineural hearing loss with tinnitus; as it grows it affects adjacent cranial nerves (V, VII). Bilateral tumours suggest neurofibromatosis type 2.
Recognise
- Unilateral sensorineural hearing loss + tinnitus (the key early features) ± vertigo/imbalance
- Larger: facial numbness (CN V, absent corneal reflex), facial weakness (CN VII), cerebellar signs
- Bilateral vestibular schwannomas = neurofibromatosis type 2
Red flags
- Any asymmetric/unilateral sensorineural hearing loss → MRI to exclude this; brainstem compression if large
Differentials & how to tell them apart
Investigations
MRI of the internal auditory meatus/cerebellopontine angle (the diagnostic test); pure-tone audiometry (asymmetric sensorineural loss).
Management
MRI to diagnose; manage by size — observe, microsurgery, or stereotactic radiosurgery
- 1Asymmetric sensorineural hearing loss → MRI of the cerebellopontine angle. Manage by size/growth/symptoms: serial observation, stereotactic radiosurgery, or microsurgical excision.Gate: Any UNILATERAL/asymmetric sensorineural hearing loss should be imaged (MRI) to exclude a vestibular schwannoma — do not attribute it to age
- 2Bilateral tumours → investigate for neurofibromatosis type 2 (genetics); monitor facial-nerve function with treatment.
Key points
Unilateral sensorineural hearing loss + tinnitus = image the CPA. Bilateral = NF2. Distinguish from Ménière (episodic vertigo + aural fullness, no mass).
Monitor & prognosis
Hearing, facial-nerve function, tumour growth on serial MRI.
Benign and slow-growing; good outcomes with timely treatment.
Source: NICE CKS (hearing loss); ENT/neurosurgery