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Activating mutations in the MAP-kinase pathway define non-ossifying fibroma of bone.

Daniel BaumhoerMichal KovacJan SperveslageBaptiste AmelineAnna-Christina StroblArthur KrauseMarcel TrautmannEva WardelmannMichaela NathrathSylvia HöllerJendrik HardesGeorg GoshegerAndreas H KriegVolker ViethRoberto TiraboscoFernanda AmaryAdrienne M FlanaganWolfgang Hartmann
Published in: The Journal of pathology (2019)
Non-ossifying fibroma (NOF), which occasionally results in pathologic fracture, is considered the most common benign and self-limiting lesion of the growing skeleton. By DNA sequencing we have identified hotspot KRAS, FGFR1 and NF1 mutations in 48 of 59 patients (81.4%) with NOF, at allele frequencies ranging from 0.04 to 0.61. Our findings define NOF as a genetically driven neoplasm caused in most cases by activated MAP-kinase signalling. Interestingly, this driving force either diminishes over time or at least is not sufficient to prevent autonomous regression and resolution. Beyond its contribution to a better understanding of the molecular pathogenesis of NOF, this study adds another benign lesion to the spectrum of KRAS- and MAP-kinase signalling-driven tumours. Copyright © 2018 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
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