A 7-year-old boy in otherwise good health presented with several months of altered vision, described by his parents as difficulty fixating on objects and intermittent squinting, as well as problems with depth perception causing him to trip or stumble. He had not experienced any symptoms suggestive of seizure activity. Neurologic exam revealed a right 6th cranial nerve palsy but was otherwise intact. Magnetic resonance imaging revealed a well-circumscribed, T2-hyperintense, non-enhancing, 2.5-cm ovoid mass in the inferior pons (Fig. 1 a; Supplemental Fig. 1). Stereotactic biopsy of the mass was performed. Intraoperative cytologic preparation and histologic sections revealed a low-grade glial neoplasm consisting of bland bipolar tumor cells with oval nuclei embedded in a myxoid stroma; a prominent angiocentric growth pattern was noted (Fig. 1 b; Supplemental Figs. 2 and 3). No appreciable mitotic activity, necrosis, or microvascular proliferation were identified. Rosenthal fibers and eosinophilic granular bodies were not seen. Immunostaining for glial fibrillary acidic protein (GFAP) was positive in the tumor cells with accentuated perivascular staining. The Ki-67 labeling index was estimated at 2%. Immunostaining for IDH1-R132H and histone H3-K27M mutant proteins was negative. While the histologic features were considered most suggestive of pilomyxoid astrocytoma, targeted next-generation sequencing was performed on the UCSF500 Cancer Panel as previously described to help clarify the diagnosis [4]. This revealed an interstitial deletion on chromosome 6q with 5′ breakpoint in the MYB gene and 3′ breakpoint in the QKI gene (Fig. 1 c), resulting in an MYB-QKI gene fusion. Sequencing reads demonstrated a fusion junction between intron 15–16 of MYB and intron 4–5 of QKI (Fig. 1 d, e), predicted to result in an in-frame fusion protein where the N-terminal portion is composed

Angiocentric glioma is defined in the 2016 WHO Classification as “an epilepsy-associated, stable or slow-growing cerebral tumor primarily affecting children and young adults; histologically characterized by an angiocentric pattern of growth, monomorphous bipolar cells, and features of ependymal differentiation”[5]. Since its initial description by Wang et al.[8], fewer than 100 cases have been reported, nearly all of which were epilepsy-associated tumors located in the cerebral cortex [1, 8]. Recently, an in-frame MYB-QKI gene fusion was identified as the defining genetic alteration in the majority of tumors pathologically classified as angiocentric gliomas [2, 6]. To date, only rare examples of angiocentric glioma-like tumors located outside of the cerebral hemispheres have been reported, but none have been genetically characterized [3, 7]. Here we report the case of a young child with 6th cranial nerve palsy due to an angiocentric glioma with MYB-QKI fusion centered in the pons; as such, the definition of this tumor type should not be restricted to