Malignant peripheral nerve sheath tumor


A malignant peripheral nerve sheath tumor is a form of cancer of the connective tissue surrounding peripheral nerves. Given its origin and behavior it is classified as a sarcoma. Neurofibromatosis type 1 is a risk factor for developing MPNSTs. The lifetime risk for an MPNST in patients with NF-1 is 8–13%. MPNST with rhabdomyoblastomatous component are called malignant triton tumors.
The first-line treatment is surgical resection with wide margins. Chemotherapy and often radiotherapy are done as adjuvant and/or neoadjuvant treatment depending upon various risk factors.

Signs and symptoms

Symptoms may include:
  • Swelling around the tumor
  • Difficulty in moving the extremity that has the tumor, including a limp.
  • Soreness localized to the area of the tumor or in the extremity.
  • Neurological symptoms.
  • Pain or discomfort: numbness, burning, or "pins and needles".
  • Dizziness and/or loss of balance.

    Causes

Soft tissue sarcomas have been linked within families, so it is hypothesized that neurofibrosarcoma may be genetic, although researchers still do not know the exact cause of the disease. Evidence supporting this hypothesis includes loss of heterozygosity on the 17p chromosome. The p53 genome on 17p in neurofibrosarcoma patients is mutated, increasing the probability of cancer. The normal p53 gene will regulate cell growth and inhibit any uncontrollable cell growth in the healthy population; since p53 is inactivated in neurofibrosarcoma patients, they are much more susceptible to developing tumors.

Genetics

A malignant peripheral nerve sheath tumor is rare, but is one of the most common non-rhabdomyosarcoma soft tissue sarcomas in the pediatric population. Neurofibromatosis type 1 is a risk factor for developing MPNSTs. NF-1 is a genetic disorder caused by a mutation on chromosome 17. The lifetime risk of patients with NF-1 developing MPNSTs has been estimated at 8–13%, with a yearly risk of developing MPNSTs of 0.16% compared to 0.001% in the general population.

Diagnosis

The most conclusive test for a patient with a potential neurofibrosarcoma is a tumor biopsy. MRIs, X-rays, CT scans, and bone scans can aid in locating a tumor and/or possible metastasis.

Classification

Malignant peripheral nerve sheath tumors are a rare type of cancer that arise from the soft tissue that surrounds nerves. They are a type of sarcoma. Most malignant peripheral nerve sheath tumors arise from the nerve plexuses that distribute nerves into the limbs—the brachial and lumbar plexuses—or from nerves as they arise from the trunk.

Treatment

Treatment for neurofibrosarcoma is similar to that of other cancers.
Surgery is an option; the removal of the tumor along with surrounding tissue may be vital for the patient's survival. For discrete, localized tumors, surgery is often followed by radiation therapy of the excised area to reduce the chance of recurrence.
For patients who have neurofibrosarcomas in an extremity, if the tumor is vascularized and has many nerves going through it and/or around it, amputation of the extremity may be necessary. Some surgeons argue that amputation should be the procedure of choice when possible, due to the increased chance of a better quality of life. Otherwise, surgeons may opt for a limb-saving treatment, by removing less of the surrounding tissue or part of the bone, which is replaced by a metal rod or grafts.
Radiation will also be used in conjunction with surgery, especially if the limb was not amputated. Radiation is rarely used as a sole treatment.
In some instances, the oncologist may choose chemotherapy drugs when treating a patient with neurofibrosarcoma, usually in conjunction with surgery. Patients taking chemotherapy must be prepared for the side effects that come with any other chemotherapy treatment, such as; hair loss, lethargy, weakness, etc.

Prognosis

Patient response to treatment will vary based on age, health, and the tolerance to medications and therapies.
Metastasis occurs in about 39% of patients, most commonly to the lung. Features associated with poor prognosis include a large primary tumor, high grade disease, co-existent neurofibromatosis, and the presence of metastases.
It is a rare tumor type, with a relatively poor prognosis in children.
In addition, MPNSTs are extremely threatening in NF1. In a 10-year institutional review for the treatment of chemotherapy for MPNST in NF1, which followed the cases of 1 per 2,500 in 3,300 live births, chemotherapy did not seem to reduce mortality, and its effectiveness should be questioned. Although with recent approaches with the molecular biology of MPNSTs, new therapies and prognostic factors are being examined.