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Malignant Peripheral Nerve Sheath Tumors (MPNST)
Malignant peripheral nerve sheath tumors (MPNSTs) are sarcomas which originate from peripheral nerves or from cells associated with the nerve sheath, such as Schwann cells, perineural cells, or fibroblasts. Because MPNSTs can arise from multiple cell types, the overall appearance can very greatly from one case to the next. This can make diagnosis and classification somewhat difficult. In general, a sarcoma arising from a peripheral nerve or a neurofibroma is considered to be a MPNST. The term MPNST replaces a number of previously used names including malignant schwannoma, neurofibrosarcoma, and neurogenic sarcoma.
A sarcoma is defined as a MPNST when at least one of the following criteria is met:
Dr. David Geller at the and Harvard Orthopaedic Surgery Program and Dr. Gebhardt, Frederick W. and Jane M. Ilfeld Professor of Orthopedic Surgery at Harvard Medical School, have written and in-depth article about Malignant Peripheral Nerve Sheath Tumors (MPNST) for the Electronic Sarcoma Update Newsletter (ESUN). Their article gives an extensive set of references to articles dealing with this disease. We are grateful to them for writing this informative article. Click on the above link to view it.
There are over 50 subtypes of sarcoma. The American Cancer Society's 2005 Key Statistics About Sarcoma states that the most common types of soft tissue sarcoma are: MFH or Malignant Fibrous Histiocytoma (28%), liposarcoma (15%), LMS or leiomyosarcoma (12%), synovial sarcoma (10%), malignant peripheral nerve sheath tumors (6%), and rhabdomyosarcoma (5%). All of the other types of soft tissue sarcoma occur at percentages of 3% or less.
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