Malignant peripheral nerve sheath tumors in schwannomatosis: systematic review and meta-analysis
MPNSTs, although rare in schwannomatosis, can arise even in the absence of prior radiation exposure and may mimic benign schwannomas. A preliminary risk stratification tool may aid in identifying high-risk patients and optimizing treatment approaches, although validation is needed. Given the aggressive nature of MPNSTs and their potential for delayed diagnosis due to their rarity, vigilant monitoring and individualized treatment strategies are crucial. Future research should focus on refining risk prediction models and exploring targeted therapies for schwannomatosis-associated MPNSTs to improve patient outcomes.
Authors
- Chloe Gui (ORCID: https://orcid.org/0000-0002-6685-1970)
- Suganth Suppiah (ORCID: https://orcid.org/0000-0003-4569-0466)
- Ken Porche (ORCID: https://orcid.org/0000-0002-2616-5853)
- Kirsten M. Hayford
- Robert J. Spinner
Institutions
- University Health Network (CA)
- Mayo Clinic (US)
- University of Toronto (CA)
- Mayo Clinic in Florida (US)
Publication Details
- Journal
- Journal of neurosurgery
- Published
- 2025-11-15
- DOI
- https://doi.org/10.3171/2025.6.jns251508
- Primary Topic
- Neurofibromatosis and Schwannoma Cases
- Type
- article
- Field-Weighted Citation Impact
- 0.00