What kind of tumor is an acoustic neuroma?
Acoustic neuromas, also known as vestibular schwannomas, are benign tumors that arise from the cochleovestibular (hearing and balance) nerve. Over 5,000 of these tumors are diagnosed in the United States per year.
How are acoustic neuromas treated at Johns Hopkins?
Post-surgical treatment for acoustic neuromas (Vestibular Schwannomas) After treatment for acoustic neuroma, some patients experience hearing loss, cerebrospinal fluid leak, damage to the nerves in the face and other problems. Johns Hopkins offers comprehensive surgical treatment and rehabilitation care for all of these problems.
Who is the leader of acoustic neuromas in the US?
A couple evenings of educating myself helped me be as clear-headed (no pun intended) as possible.” Peter’s doctor had suggested he start by seeing Dr. Samuel Selesnick, an o tolaryngologist who is a leader in the field of acoustic neuromas.
How are acoustic neuroma and vestibular schwannoma treated?
The terms “acoustic neuroma” and “vestibular schwannoma” mean the same thing. It is a rare tumor that often affects middle-aged people. Acoustic neuroma (vestibular schwannoma) is diagnosed using hearing tests and imaging tests. Treatment can include observation (watching and waiting), surgery or radiation.
How is acoustic neuroma treated at Mayo Clinic?
Acoustic neuroma usually arises from the Schwann cells covering this nerve and grows slowly or not at all. Rarely, it may grow rapidly and become large enough to press against the brain and interfere with vital functions. Treatments for acoustic neuroma include regular monitoring, radiation and surgical removal. Acoustic neuroma care at Mayo Clinic
When to have Gamma Knife surgery for acoustic neuroma?
The indications for gamma knife surgery for this tumor vary. Some physicians advocate gamma knife surgery in medically high risk patients, patients who refuse microsurgery, and in patients with post-operative residual tumor.
What kind of neuroma is bilateral vestibular schwannoma?
Bilateral vestibular schwannomas affect both hearing nerves and are usually associated with a genetic disorder called neurofibromatosis type 2 (NF2). Half of affected individuals have inherited the disorder from an affected parent and half seem to have a mutation for the first time in their family.