Abstract
The pathogenesis of neurofibromas is poorly understood outside of neurofibromatosis (NF). The BRAF proto-oncogene has been implicated in malignant peripheral nerve sheath tumors (PNSTs), however its role in neurofibromas has not been described. In this study, we identify a BRAF mutation in a 61-year old non-NF patient with a history of sporadic and recurrent neurofibromas localized to the right upper extremity. Despite repeat resections to establish local control, he developed median nerve neuropathy secondary to a 13 × 4 cm plexiform neurofibroma. Genetic sequencing of the neurofibroma revealed the expression of a novel BRAF L597Q mutation. This study is the first to describe the BRAF L597Q mutation in PNSTs and the first to implicate a BRAF mutation in neurofibroma biology. We hypothesize that BRAF mutations may identify a molecularly-distinct subset of recurrent neurofibromas and may provide potential for targeted therapeutics.
| Original language | English |
|---|---|
| Pages (from-to) | 276-278 |
| Number of pages | 3 |
| Journal | Experimental and Molecular Pathology |
| Volume | 103 |
| Issue number | 3 |
| DOIs | |
| State | Published - Dec 2017 |
Keywords
- BRAF
- Neurofibroma
- Peripheral nerve sheath tumors