Abstract
A benign (WHO grade I), relatively circumscribed, biphasic cerebral neoplasm occurring predominantly in the temporal lobe and most commonly affecting young adults. No population-based epidemiologic data are available to date. Papillary glioneuronal tumor (PGNT) was initially described as “pseudopapillary ganglioglioneurocytoma” or “pseudopapillary neurocytoma with glial differentiation.” Established as a distinct clinicopathologic entity in 1998 by Komori et al. Regarded as a variant of ganglioglioma in the 2000 WHO classification of central nervous system tumors. Recently added as a new entity in the 2007 WHO classification.
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Rivera-Zengotita, M., Illner, A., Adesina, A.M. (2010). Papillary Glioneuronal Tumor. In: Adesina, A., Tihan, T., Fuller, C., Poussaint, T. (eds) Atlas of Pediatric Brain Tumors. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-1062-2_20
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DOI: https://doi.org/10.1007/978-1-4419-1062-2_20
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