Gliomas arising in the setting of neurofibromatosis type 1

Representative scanned pathology slides from 47 patients with gliomas arising in the setting of germline NF1 mutation/deletion (i.e. neurofibromatosis type 1). Included are hematoxylin and eosin stained sections and representative immunohistochemical stains from the 47 tumors. These were scanned on an Aperio digital slide scanner, and the .SVS files can be viewed using the freely downloadable ImageScope software from Leica Biosystems. The complete clinical, histopathologic, genetic, and epigenomic features of these 47 cases are described in detail in the following report: Lucas CG, et al. Multiplatform molecular analyses refine classification of gliomas arising in patients with neurofibromatosis type 1. Acta Neuropathologica 2022 Aug 9. doi: 10.1007/s00401-022-02478-5. Online ahead of print. PMID: 35945463