Early detection of Vestibular Schwannoma may be difficult due to subtle symptoms that the person may not realize. MRI with contrast is the best way to visualize this pathology but CT may also be used.
Unilateral Vestibular Schwannoma accounts for about 8% of all skull tumors. Symptoms may occur at any age but they usually appear anywhere from 30 to 60 years old. Bilateral Vestibular Schwannoma affects both hearing nerves and may be associated with a genetic disorder called Neurobibromatosis Type 2. Some scientists believe that unilateral and bilateral Vestibular Schwannoma comes from a loss of function of the gene on chromosome 22. This has an affect on the production of Schwann cells.
Treatment may be, but not limited to, surgical removal, radiation, and monitoring. The majority of cases where patients have Vestibular Schwannoma, the tumor is surgically removed. Sometimes, the growth is growing over the nerve and the nerve will have to be removed as well. This can make symptoms worse and a patient will not be able to recover from this. Radiation may be used to reduce the size and growth if the tumor to prevent it from getting bigger and causing further complications. The last is monitoring. Sometimes the growth is not worth removing if it is not causing harmful symptoms to the patient. At this point, they monitor the growth to see if it is progressively getting worse.
National Institute on Deafness and Other Communication Disorders (June, 2010) Vestibular schwannoma (acoustic neuroma) & neurofibromatosis. Retrieved from http://nidcd.nih.gov/health/hearing/acoustic_neuroma.html
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