
Vestibular schwannoma
What is a Vestibular Schwannoma?
A vestibular schwannoma, sometimes referred to as acoustic neuroma, is a benign tumor found on the vestibularcochlear nerve, the nerve that connects the ear to the brain. This nerve is behind the ear, right under the brain. This type of tumor is typically very slow- growing, and it may press against the nerves controlling hearing and balance as it grows. An acoustic neuroma is an uncommon cause of hearing loss. If the tumor remains small, many patients will remain asymptomatic. However, if it enlarges enough to exert serious pressure on the brain, it may become life-threatening.
Causes of a Vestibular Schwannoma
Most of the time, the cause of a vestibular schwannoma is unknown. If vestibular schwannomas develop in both auditory nerves, the underlying cause may be a heredity disorder known as neurofibromatosis type 2, but this genetic defect accounts for only a very small percentage of cases. The vast majority of vestibular schwannomas are sporadic (non-inherited).
Symptoms of Vestibular Schwannoma
Many patients with small vestibular schwannomas will not be symptomatic. As it grows, it presses against the hearing and balance nerves, and large tumors may press against the brain and brainstem. Pressures on these structures generates symptoms. These symptoms may include:
- Loss of hearing in one ear
- Balance problems
- Ringing in the ears, also known as tinnitus
- Difficulty swallowing and hoarseness
- Headaches
- Clumsiness or unsteadiness
- Confusion
- Numbness
- Facial paralysis
Diagnosis of a Vestibular Schwannoma
There are several ways a physician may diagnose a vestibular schwannoma. The physician may evaluate the ears, balance system, and mobility of the face. It is possible, however, that there will be no physical evidence of the tumor. The following diagnostic tests may be administered to detect the presence of a vestibular schwannoma.
- Hearing test (audiogram)
- Auditory brain stem response, or ABR
- Electronystagmography (ENG) or videonystagmography (VNG)
- MRI scan of the brain
Treatment of a Vestibular Schwannoma
When a vestibular schwannoma remains small, the patient may only need regular checkups and surveillance for growth. Tumors that demonstrate active growth may require treatment with radiation or surgical removal. Radiation is designed to halt tumor growth while surgery facilitates tumor removal. The decision of which treatment to pursue is dependent on many factors, which will be discussed in depth between the patient and the physician.
Risks of Treatment for Vestibular Schwannoma
There are risks associated with both radiation and surgery for treatment of a vestibular schwannoma. With radiosurgery, risks may include partial or total hearing loss in the affected ear, dizziness, facial weakness, or brain swelling.
If typical surgery is required for the treatment of a vestibular schwannoma, risks may include:
- Infection
- Bleeding
- Leakage of cerebrospinal fluid
- Facial nerve paralysis
- Tinnitus
- Hearing loss
- Brain complications
Ear Surgery
Hearing loss
Cochlear Implants
Swimmer’s ear
Surfer’s Ear
Meniere’s disease
Inner ear disorders
Benign paroxysmal positional vertigo (BPPV)
Tinnitus
Dizziness and Motion Sickness
Tympanoplasty
Ossicular Reconstrution
Myringoplasty
Bone-anchored hearing aid (BAHA)
Cauliflower Ear (Auricular Hematoma)
Cerebrospinal Fluid Leak
Cholesteatoma
Cochlear Implantation
Earmolds
Ear canal stenosis and atresia
Ear infections
Earwax
Vestibular schwannoma
