Schwannoma

What causes schwannomas?

In most cases, it is not known why a schwannoma develops. In some cases, a schwannoma develops in association with an underlying genetic disorder such as neurofibromatosis 2 (NF2), schwannomatosis, or Carney complex. These disorders may cause multiple tumors to develop. When a schwannoma is a feature of a genetic disorder, it is caused by a genetic mutation that causes an increased risk for tumor growth.

Schwannomas develop from the Schwann cells which normally form a protective lining around most of the nerves of the peripheral nervous system and also the nerve root. The peripheral nervous system carries signals from the brain and spinal cord (central nervous system) to the muscles and tissues of the body. The nerve root is the first part of nerve leaving the spinal cord and then becomes a peripheral nerve. Schwann cells provide support by wrapping around nerves and nerve roots but also produce the fatty insulation called myelin that surrounds nerves and helps nerve signals travel fast. When a schwannoma grows large enough, it may begin compressing or putting a squeezing pressure on the nerve. It also damages the myelin in that area of the nerve. Together the compression of the nerve and myelin damage cause the symptoms related to schwannomas.

Last updated on 05-01-20

How is a schwannoma diagnosed?

A schwannoma may be difficult to diagnosis at first because, depending on its location, the symptoms it causes may be similar to the symptoms caused by other health problems. The following tests may be used to rule out other causes of the symptoms and confirm the diagnosis:

  • X-ray
  • Ultrasound
  • CT scan
  • Magnetic resonance imaging (MRI) - MRI can help determine if a tumor is on the outside of a nerve or part of a nerve and if it involves other nearby structures
  • Biopsy of the tumor to confirm the diagnosis - a biopsy involves removing a small sample of the schwannoma to be examined under the microscope

In some cases, a schwannoma is discovered incidentally (by chance) when a person has imaging studies for another reason.

Last updated on 05-01-20

Are schwannomas inherited?

Most schwannomas are not inherited. The vast majority occur by chance and as a single tumor.

In some cases, a person develops a schwannoma (or multiple schwannomas) due to having an underlying genetic disorder such as neurofibromatosis 2 (NF2), schwannomatosis, or Carney complex. These disorders are inherited in an autosomal dominant manner. This means that having a change (mutation) in only one copy of the responsible gene in each cell is enough to cause features of the condition.

In some cases, a person with an autosomal dominant disorder inherits the mutation from a parent with the disorder. In other cases, the mutation occurs for the first time in a person with no family history of the condition. This is called a de novo mutation.

When a person with a mutation that causes an autosomal dominant disorder has children, each of his/her children has a 50% (1 in 2) chance to inherit that mutation.

Last updated on 05-01-20

How might a schwannoma be treated?

Treatment for a schwannoma may depend on the location of the tumor, severity of symptoms, and whether the tumor is benign or malignant (cancerous). A benign schwannoma causing symptoms or affecting a person's appearance is typically treated with surgery to remove as much as the tumor as possible, while keeping the affected nerve intact. It is often possible to remove the entire tumor. Surgery usually quickly relieves the related symptoms, although if muscle weakness was present before surgery, the muscle may not return to full strength.

Treatment for a malignant schwannoma may involve both surgery and radiation therapy.

Last updated on 05-01-20

Name: American Cancer Society 250 Williams Street NW
Atlanta, GA, 30329, United States
Toll Free: 1-800-227-2345 Url: https://www.cancer.org
Name: American Brain Tumor Association 8550 W. Bryn Mawr Ave, Ste 550
Chicago, IL, 60631, United States
Phone: +1-773-577-8750 Toll Free: 1-800-886-2282 Fax : +1-773-577-8738 Email: info@abta.org Url: https://www.abta.org/
Van Abel KM, Carlson ML, Link MJ, Neff BA, Beatty CW, Lohse CM, Eckel LJ, Lane JI, Driscoll CL. Primary inner ear schwannomas: a case series and systematic review of the literature Laryngoscope. 2013; 123(8). 1957-1966. Reference Link Schwannoma Cancer Research UK. July 1, 2013; Reference Link Dickey ID. Neurilemmoma Medscape Reference. August 18, 2016; Reference Link

Connect with other users with Schwannoma on the RareGuru app

Do you have information about a disease, disorder, or syndrome? Want to suggest a symptom?
Please send suggestions to RareGuru!

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

People Using the App

Join the RareGuru Community

To connect, share, empower and heal today.

People Using the App