Malignant peripheral nerve sheath tumor (MPNST) is a rare cancer type that affects the protective tissue that surrounds the nerves that come out the spinal cord into the different parts of the body (peripheral nerves). These are the nerves that are outside the central nervous system. The presence of the tumor can cause a lump in the skin, pain in the area and weakness of movement in the affected part. These tumors can spread (metastasize) to other areas of the body.
They are considered aggressive tumors because there is a high proportion of recurrence, the tumor is able to come back after it has been removed, and it is able to extend and invade other parts of the body (usually the lungs).
Malignant peripheral nerve sheath tumor (MPNST) is a rare cancer type that affects the protective tissue that surrounds the nerves that come out the spinal cord into the different parts of the body (peripheral nerves). These are the nerves that are outside the central nervous system. The presence of the tumor can cause a lump in the skin, pain in the area and weakness of movement in the affected part. These tumors can spread (metastasize) to other areas of the body.
They are considered aggressive tumors because there is a high proportion of recurrence, the tumor is able to come back after it has been removed, and it is able to extend and invade other parts of the body (usually the lungs).
MPNST is sometimes found in association with another disorder called neurofibromatosis type 1. The frequency of MPNST alone in the general population is about one per 1100,000 individuals.
Name | Abbreviation |
---|---|
Malignant Peripheral Nerve Sheath Tumors | MPNST |
The underlying cause is the appearance of mutations in the cells that form the tissue lining the nerves. These mutations make them grow uncontrollably, but no particular type of genetic alteration has been linked to MPNST. However, there are some risk factors associated with the development of MPNST:
The application of radiation therapy to treat another cancer might cause the development of MPNST in the area decades after its administration
The presence of benign nerve tumors
Individuals that suffer from neurofibromatosis type I are more prone to develop MPNSTs
As these tumors can spread (metastasize) to other areas of the body, they may be removed surgically. Radiation therapy is used to decrease the chance of recurrence. Chemotherapy may be used if the tumor cannot be completely removed by surgery.
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