Superficial, typically temporal lobe-located glioneuronal (mixed neuronal-glial) tumor that tends to present in male patients < 20 y.o. and manifest with refractory partial-onset seizures (Differential includes ganglioglioma/gangliocytoma).
They typically localize to the cortical/juxtacortical region of the temporal lobe.
They are generally benign (G1) and do not cause mass effect or enhance.
Surgical resection often helps in seizure management.
Histopathology characteristically demonstrates floating neurons (a mature ganglion cell in a pool of mucin) and also oligodendroglia-like cells (fried-egg appearance).
References
Adesina, Adekunle M., Tarik Tihan, Christine E. Fuller, and Tina Young Poussaint. Atlas of Pediatric Brain Tumors. Springer, 2016.
Gray, Frangoise, Charles Duyckaerts, and Umberto De Girolami. Escourolle and Poirier’s Manual of Basic Neuropathology. OUP USA, 2013.
Tonn, Jörg-Christian, Manfred Westphal, and J. T. Rutka. Oncology of CNS Tumors. Springer Science & Business Media, 2010.
Yachnis, Anthony T., and Marie L. Rivera-Zengotita. Neuropathology E-Book: A Volume in the High Yield Pathology Series. Elsevier Health Sciences, 2012.
Image Reference
Histopathology: Floating Neurons and Oligodendroglia-like Cells
Jensflorian. English: Dysembryoblastic Neuroepithelial Tumor (DNET), MAP2 Immunohistochemistry High Magnification, FFPE Specimen. April 14, 2015. Own work. https://commons.wikimedia.org/wiki/File:DNET_MAP-high_power.jpg.