• Sarcoma Subtype Information
• Alveolar Soft Part Sarcoma (ASPS)
• Angiosarcoma
• Chondrosarcoma
• Dermatofibrosarcoma Protuberans (DFSP)
• Desmoid Sarcoma
• Ewing’s Sarcoma
• Fibrosarcoma
• Gastrointerstinal Stromal Tumor (GIST)
• Non-Uterine Leiomyosarcoma
• Liposarcoma
• Malignant Fibro Histiocytoma (MFH)
• Malignant Peripheral Nerve Sheath Tumor (MPNST)
• Uterine Leiomyosarcoma
• Osteosarcoma
• Rhabdomyosarcoma
• Synovial Sarcoma
The malignant peripheral nerve sheath tumor (MPNST) is the malignant counterpart to benign soft tissue tumors such as neurofibromas and schwannomas. This term is preferred to older designations such as malignant schwannomas and neurofibrosarcomas. It is most common in the deep soft tissue, usually in close proximity of a nerve trunk. The most common sites include the sciatic nerve, brachial plexus, and sarcal plexus. The most common symptom is pain which usually prompts a biopsy. Most cases average more than 5 cm in diameter. On sections, it may have a white surface with areas of necrosis or hemorrhage. It is the most common sarcoma arising in the setting of von Recklinghausen’s disease.
10% of all soft tissue sarcomas seen in consultation with 50% occurring in the setting of neurofibromatosis I.
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Patient Resources
Information on sarcoma subtypes, treatments, clinical trials, and other important resources for sarcoma patients and families.
Sarcoma Patient Registry
Information on the Sarcoma Patient Registry. If you are diagnosed with sarcoma, please consider joining the Registry.
Research Grants
Information on applying for a sarcoma research grant, current research funded by the SFA, and past research grants.