Acoustic schwannomas (also known as vestibular schwannomas) are relatively common tumours that arise from the vestibulocochlear nerve (CN VIII) and represent ~80% of cerebellopontine angle masses. Bilateral acoustic schwannomas are strongly suggestive of neurofibromatosis type 2 (NF2).
These tumours classically present on imaging as a solid nodular mass with an intracanalicular component that often results in widening of the porus acusticus. They usually show intense contrast enhancement and, when larger, cystic degeneration can be present. Haemorrhagic areas may also be seen, but calcification is typically not present.
They account for 7-8% of all primary intracranial tumours 2 and 75-90% of cerebellopontine angle masses 1-2,8. 95% of solitary lesions are sporadic. Bilateral vestibular schwannomas are highly suggestive of neurofibromatosis type 2 (NF2), although bilateral tumours are encountered in the familial form of acoustic schwannomas in the absence of other stigmata of NF2 5.
The typical presentation is with adult-onset sensorineural hearing loss or tinnitus. In some patients, this goes unnoticed, and presentation is delayed until the lesion is much larger and presents with symptoms related to mass effect. Possibilities include cerebellar and brainstem symptoms (e.g. cranial nerve dysfunction other than vestibulocochlear), or hydrocephalus due to the effacement of the fourth ventricle.
Acoustic schwannomas are benign tumours (WHO grade 1), which usually arise from the intracanalicular segment of the vestibular portion of the vestibulocochlear nerve (CN VIII) 2,4, near the transition point between glial and Schwann cells (Obersteiner-Redlich zone) 8. In over 90% of cases, these tumours arise from the inferior division of the vestibular nerve 8.
They are well-circumscribed encapsulated masses which, unlike neuromas, arise from but are separate from nerve fibres 7, which they usually splay and displace rather than engulf.
They can display two types of growth pattern:
- elongated cells with cytoplasmic processes arranged in fascicles 7
- little stromal matrix
- Verocay bodies: nuclear-free zones of processes lying between regions of nuclear palisading
- loose meshwork of cells
- less densely cellular
- microcysts and myxoid change
Most vestibular schwannomas have an intracanalicular component, and often result in widening of the porus acusticus resulting in the trumpeted IAM sign, which is present in up to 90% of cases 5. In a minority of cases (~20%) they are purely extra canalicular, only abutting the porus acusticus 1,5. Usually, there is a small CSF cap between the intracanalicular portion and the cochlea; Occasionally, these tumours grow laterally through the cochlea (transmodiolar) or vestibule (transmacular) into the middle ear. Rarely they are small and confined to the vestibule (intravestibular) or the cochlea (intracochlear) or both (vestibulocochlear) 4.
Extracanalicular extension into the cerebellopontine angle (path of least resistance) can lead to "ice cream cone" appearance.
Small tumours tend to be solid whereas cystic degeneration is seen commonly in larger tumours 2. Haemorrhagic areas may also be seen. Calcification is typically not present.
May show erosion and widening of the internal acoustic canal. The density of these tumours on non-contrast imaging is variable, and often they are hard to see, especially on account of beam hardening and streak artefact from the adjacent petrous temporal bone.
Contrast enhancement is present but can be underwhelming, especially in larger lesions with cystic components.
- slightly hypointense to adjacent brain (63%) 2
- isointense to adjacent brain (37%) 2
- may contain hypointense cystic areas
- heterogeneously hyperintense to adjacent brain 5
- fluid intensity cystic areas
- may have associated peritumoural arachnoid cysts 3
T1 C+ (Gd)
- contrast enhancement is intense
- however, heterogeneous in larger tumours
Linear enhancement may not indicate tumour, but if there is a nodular enhancement, suspect tumour recurrence (requires follow-up MRI).
Treatment and prognosis
There is variability in the rate of growth of these tumours, and as such, the decision to treat requires consideration of patient's age and co-morbidities. The options include 6 :
- observation and follow-up
- stereotactic radiosurgery
- microsurgery: number of approaches are possible, including 8:
- retrosigmoid (trans-meatal) (suboccipital)
- able to preserve hearing
- can be used for large tumours
- limited view of the internal auditory canal
- has a greater chance of residual tumour (in the lateral aspect of internal auditory canal)
middle cranial fossa
- best for small intracanalicular tumours
- able to preserve hearing
- careful skeletonisation of the facial nerve required (i.e. intraoperative facial nerve monitoring by needle electromyography with continuous stimulation)
- loss of hearing guaranteed
- retrosigmoid (trans-meatal) (suboccipital)
Overall tumour recurrence is low, ranging between 1 and 9% 8.
The most frequent differentials to be considered are:
- usually more homogeneous in appearance: significant signal heterogeneity with cystic or haemorrhagic areas is more typical of vestibular schwannoma than meningiomas (although cystic meningiomas do occur)
- meningiomas tend to have a broad dural base
- usually lack the trumpeted internal acoustic meatus sign
- calcification more common
- no enhancing component
- very high signal on DWI
- does not widen the internal auditory canal
- usually does not remodel the internal auditory canal, as metastases are usually present for only a short time
- centred on the fourth ventricle
- does not extend into the internal auditory canal
- usually younger patients
What the surgeon wants to know
In addition to general remarks about the size and location of the tumour, significant findings that influence surgical management include 8:
- how close to the fundus of the IAC the tumour reaches
- anatomical variations
- 1. Dähnert W. Radiology review manual. Lippincott Williams & Wilkins. (2003) ISBN:0781738954. Read it at Google Books - Find it at Amazon
- 2. Mulkens TH, Parizel PM, Martin JJ et-al. Acoustic schwannoma: MR findings in 84 tumors. AJR Am J Roentgenol. 1993;160 (2): 395-8. AJR Am J Roentgenol (abstract) - Pubmed citation
- 3. Tali ET, Yuh WT, Nguyen HD et-al. Cystic acoustic schwannomas: MR characteristics. AJNR Am J Neuroradiol. 14 (5): 1241-7. AJNR Am J Neuroradiol (abstract) - Pubmed citation
- 4. Mafee MF, Lachenauer CS, Kumar A et-al. CT and MR imaging of intralabyrinthine schwannoma: report of two cases and review of the literature. Radiology. 1990;174 (2): 395-400. Radiology (abstract) - Pubmed citation
- 5. Morantz RA, Walsh JW. Brain tumors, a comprehensive text. Informa HealthCare. (1994) ISBN:0824788265. Read it at Google Books - Find it at Amazon
- 6. Naumann HH, Jahrsdoerfer R, Helms J. Head and neck surgery. George Thieme Verlag. (1996) ISBN:0865776601. Read it at Google Books - Find it at Amazon
- 7. Kumar V, Abbas AK, Fausto N et-al. Robbins and Cotran pathologic basis of disease. W B Saunders Co. (2005) ISBN:0721601871. Read it at Google Books - Find it at Amazon
- 8. Silk PS, Lane JI, Driscoll CL. Surgical approaches to vestibular schwannomas: what the radiologist needs to know. Radiographics. 2009;29 (7): 1955-70. doi:10.1148/rg.297095713 - Pubmed citation
- 9. Wu EH, Tang YS, Zhang YT et-al. CT in diagnosis of acoustic neuromas. AJNR Am J Neuroradiol. 7 (4): 645-50. AJNR Am J Neuroradiol (abstract) - Pubmed citation
- 10. Fortnum H, O'Neill C, Taylor R et-al. The role of magnetic resonance imaging in the identification of suspected acoustic neuroma: a systematic review of clinical and cost effectiveness and natural history. Health Technol Assess. 2009;13 (18): iii-iv, ix-xi, 1-154. doi:10.3310/hta13180 - Pubmed citation