Acoustic neuromas (vestibular schwannomas) are slow-growing, benign, intracranial, extra-axial tumors originating from the vestibulocochlear nerve.
- Originated from Schwann cells of the nerve sheath
- Usually arise in the internal auditory canal near the cerebellopontine angle
- Most are unilateral; bilaterally seen in neurofibromatosis type 2 (NF2)
- 6–10% of all intracranial tumors
- 80–90% of cerebellopontine angle tumors
- 95% of cases are unilateral.
- Present most commonly in the 5th to 6th decades, although signs and symptoms can occur earlier
- Female predominance
- 5% of acoustic neuromas are a result of NF2.
- Bilateral acoustic neuroma occurring in NF2 present before age 30 years
- 1/100,000 per year
- Asymptomatic lesions may be more common.
3,000 diagnosed annually in the United States
Etiology and Pathophysiology
- Compression of acoustic and facial nerve when located within internal acoustic canal
- Compression of brainstem, 4th ventricle, and trigeminal nerve when tumor is at the cerebellopontine angle
- Vestibular schwannomas are related to the NF2 gene and its product merlin. Merlin acts as a tumor suppressor and as a mediator of contact inhibition. Thus, deficiencies in both NF2 genes lead to vestibular schwannoma development.
- Unknown for unilateral acoustic neuroma
- NF2: bilateral acoustic neuromas
- Autosomal dominant
- Gene located on chromosome 22q11
- High-dose ionizing radiation
- Pregnancy and epilepsy may increase risk.
- There is some literature suggesting that smoking cigarettes may be protective. However, further research must be conducted to support these claims.
- No proven increase in risk of acoustic neuroma with regular use of a mobile phone
Commonly Associated Conditions
- Pregnancy may accelerate the growth of the tumor.
- Sensorineural hearing loss (unilateral), often progressive
- Sudden deafness
- Loss of speech discrimination
- Disequilibrium is common, but vertigo is less common.
- Less common
- Weakness/loss of facial muscle functions
- Headache with hydrocephalus and increased intracranial pressure
- Trigeminal nerve dysfunction when tumor is large and compressing on cranial nerve V (CN V)
- Ataxia due to cerebellar or brainstem compression from large tumor
- Exclude other causes of hearing loss (e.g., middle-ear effusion, infection, cerumen [earwax], cholesteatoma, or tympanic membrane perforation) with otoscopic exam.
- Neurologic exam of CNs
- Weber and Rinne tests to screen for sensorineural hearing loss versus conductive hearing loss
- Contralateral ear exam if you suspect NF2 (at risk for bilateral hearing loss)
- Cerebellopontine lesions
- Facial nerve schwannoma
- Epidermoid cyst
- Arachnoid cyst
- Sensorineural hearing loss
- Presbycusis (age related)
- Ménière disease
- Ototoxicity (i.e., medications)
- Viral illness (i.e., labyrinthitis)
- Autoimmune disease
- Cerebellar pathology
Diagnostic Tests & Interpretation
Initial Tests (lab, imaging)
- MRI with gadolinium (gold standard)
- Approaches 100% specificity; detects tumors starting at 2 mm
- Noncontrast T2-weighted fast spin echo MRI
- Up to 98% specificity; less expensive than MRI with gadolinium
- CT scan detects tumors as small as 1 cm; up to 37% false-negative findings; provides good information about surrounding bony structures of the tumor
- Electrophysiologic testing
- Pure tone and speech audiometry (asymmetric, high-frequency sensorineural hearing loss)
- Speech discrimination
- Stacked auditory brainstem response (ABR): 95% sensitivity and 88% specificity; however, misses approximately up to 1/3 of tumors <1.5 cm
- Standard ABR: can only detect tumors >1 cm
- Well-demarcated and encapsulated mass attached to neural structures without direct invasion
- The mass may be dense or cystic.
- Diagnostic microscopy: densely packed spindle cells (Schwann cells) mixed in with myxoid and collagenous matrix
- Antoni A will show zones of alternatively dense and sparse areas of tissue.
- Antoni B will show a loose meshwork of cells with less cellular dense tissue.
- Palisading nuclei (Verocay bodies)
- S-100 antibody immunoreactivity
- Treatment options include observation, stereotactic radiosurgery, fractionated radiotherapy, and microsurgery.
- Without intervention, 16–26% of patients require additional treatment, with 54–63% preserving functional hearing.
- With radiosurgery, only 2–4% of patients require additional treatment, and hearing preservation is accomplished in 44–66%.
- With fractionated radiotherapy, 3–7% of patients will require additional treatment; short-term hearing preservation is reported at 59–94% of patients, although long-term outcomes are not known.
- One study comparing observation to stereotactic radiosurgery demonstrated no differences in hearing preservation, hearing survival, and speech discrimination between the groups (1)[C].
- Up to 57% of acoustic neuromas may not grow or shrink without treatment.
- Up to 70% of extracanalicular tumors may never have a growth rate exceeding 2 mm/year.
Patients with NF2-associated vestibular schwannomas tend to have higher rates of surgical complications, treatment costs, and hospital stays compared to sporadic cases.
Acoustic neuromas in children typically grow at slower rates compared to adults; this affects treatment outcomes.
A greater understanding of molecular tumorigenesis has yielded novel therapies. Suggested therapies:
- Bevacizumab may induce regression of progressive schwannomas by >40% and improves hearing.
- An inhibitor of vascular endothelial growth factor (VEGF) synthesis, PTC299, is currently in phase II trials as a potential agent to treat vestibular schwannoma.
- In vitro studies have shown that trastuzumab (an ErbB2 inhibitor) reduces vestibular schwannoma cell proliferation.
Issues For Referral
All tumors should at least be monitored, even if asymptomatic.
Observation is suitable for elderly patients with contraindications to surgery and radiotherapy: Observation is more likely to preserve hearing than radiotherapy or surgery. If the patient has dizziness related to the tumor, treatment may be indicated to prevent falls.
- Gamma Knife single-dose stereotactic radiosurgery
- Performed on an outpatient basis
- For smaller tumors (<3 cm) or contraindications to microsurgery
- Shown to have better tumor control rates than observation in some studies
- Lower dose radiation has fewer complications.
- Fractionated stereotactic radiosurgery
- Delivers a higher dose of radiation and less damage to healthy tissue
- Requires multiple treatments, and total radiation dose is higher than single-dose radiation
- Suitable for all sizes of tumor
- Surgery is the recommended definitive treatment.
- Lowest rate of recurrence, with up to 97.5% complete tumor removal
- Retromastoid/retrosigmoid: can be used for all acoustic tumors
- Middle cranial fossa: for small tumors with aim of preserving hearing
- Translabyrinthine: for all but large tumors
- Transpetrous approaches are safe for acoustic neuroma removal, and the postoperative complication rate is low.
- The retrolabyrinthine approach seems to be a good hearing preservative approach, regardless of tumor volume.
- In one study, 79.1% of surgeries involved a translabyrinthine approach, with the remaining combined retrosigmoid and transtemporal (10.4%), middle fossa (6.0%), and stereotactic radiosurgery (4.5%). The highest complication rate was seen in the combined retrosigmoid and transtemporal approach cohort (2)[B].
- The introduction of endoscopy for the middle fossa approach has resulted in improved preservation of hearing and facial nerve function.
- Treatment providers should be aware that radiation treatment carries a small risk of malignant transformation (0.3% in a large series).
- Yearly MRI follow-up for slow-growing tumors is advised.
- MRI and audiometry
- In one study, composite quality of life (cQOL) score 0 to 5 years out of surgery was significantly highest among patients receiving stereotactic radiosurgery compared to microsurgery and observation. However, after 5 years, these differences were not seen.
- One study revealed that imbalance or disequilibrium may be indicative of tumor growth.
- In one study, 83% of patients who underwent acoustic neuroma resection still experienced persistent tinnitus.
- Mass effects: CN compression, hydrocephalus, brainstem compression, cerebellar tonsil herniation
- Surgical complications: hearing loss, CSF leakage, facial nerve injury, headaches, meningitis
- Bell JR, Anderson-Kim SJ, Low C, et al. The persistence of tinnitus after acoustic neuroma surgery. Otolaryngol Head Neck Surg. 2016;155(2):317–323. [PMID:27095048]
- Choi JW, Lee JY, Phi JH, et al. Clinical course of vestibular schwannoma in pediatric neurofibromatosis type 2. J Neurosurg Pediatr. 2014;13(6):650–657. [PMID:24724714]
- Fong B, Barkhoudarian G, Pezeshkian P, et al. The molecular biology and novel treatments of vestibular schwannomas. J Neurosurg. 2011;115(5):906–914. [PMID:21800959]
- Hasegawa T, Kida Y, Kato T, et al. Long-term safety and efficacy of stereotactic radiosurgery for vestibular schwannomas: evaluation of 440 patients more than 10 years after treatment with gamma knife surgery. J Neurosurg. 2013;118(3):557–565. [PMID:23140152]
- Kagoya R, Shinogami M, Kohno M, et al. Distortion-product otoacoustic emission tests evaluate cochlear function and differentiate cochlear and vestibular schwannoma. Otolaryngol Head Neck Surg. 2013;148(2):267–271. [PMID:23197675]
- Montaser AS, Todeschini AB, Harris MS, et al. Role of endoscopy in resection of intracanalicular vestibular schwannoma via middle fossa approach: technical nuances. World Neurosurg. 2018;120:395–399. [PMID:30201576]
- Plotkin SR, Stemmer-Rachamimov AO, Barker FG II, et al. Hearing improvement after bevacizumab in patients with neurofibromatosis type 2. N Engl J Med. 2009;361(4):358–367. [PMID:19587327]
- Robinett ZN, Walz PC, Miles-Markley B, et al. Comparison of long-term quality-of-life outcomes in vestibular schwannoma patients. Otolaryngol Head Neck Surg. 2014;150(6):1024–1032. [PMID:24596235]
- D33.3 Benign neoplasm of cranial nerves
- 225.1 Benign neoplasm of cranial nerves
- 126949007 acoustic neuroma (disorder)
- The most common presenting signs and symptoms are unilateral sensorineural hearing loss, poor speech discrimination, and tinnitus.
- May present as sudden deafness
- MRI with gadolinium is the diagnostic gold standard.
- The commonly used treatment options include observation, stereotactic radiosurgery, fractionated radiotherapy, and microsurgery.
Jason E. Cohn, DO
Brian McKinnon, MD, MBA, MPH, FCPP, FACS
Robert T. Sataloff, MD, DMA, FACS
- Elliott A, Hebb AL, Walling S, et al. Hearing preservation in vestibular schwannoma management. Am J Otolaryngol. 2015;36(4):526–534. [PMID:25771841]
- Olshan M, Srinivasan VM, Landrum T, et al. Acoustic neuroma: an investigation of associations between tumor size and diagnostic delays, facial weakness, and surgical complications. Ear Nose Throat J. 2014;93(8):304–316. [PMID:25181660]
- Jethanamest D, Rivera AM, Ji H, et al. Conservative management of vestibular schwannoma: predictors of growth and hearing. Laryngoscope. 2015;125(9):2163–2168. [PMID:25647714]
- Mahboubi H, Ahmed OH, Yau AY, et al. Complications of surgery for sporadic vestibular schwannoma. Otolaryngol Head Neck Surg. 2014;150(2):275–281. [PMID:24201062]
- Copeland WR, Mallory GW, Neff BA, et al. Are there modifiable risk factors to prevent a cerebrospinal fluid leak following vestibular schwannoma surgery? J Neurosurg. 2015;122(2):312–316. [PMID:25415063]
- Carlson ML, Tveiten ØV, Driscoll CL, et al. Long-term dizziness handicap in patients with vestibular schwannoma: a multicenter cross-sectional study. Otolaryngol Head Neck Surg. 2014;151(6):1028–1037. [PMID:25273693]
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