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Histopathology of Adult and Pediatric Glioblastoma

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Precision Molecular Pathology of Glioblastoma

Part of the book series: Molecular Pathology Library ((MPLB))

Abstract

Glioblastomas (GBMs) are the most common overall malignant primary brain tumor, with 3.23 cases per 100,000 in the adult population. In children, they are much less common, with a reported incidence of 0.14 cases per 100,000. The prognosis of these high-grade tumors is typically poor and most patients succumb to their disease within a few years. Most of these tumors occur sporadically; although rare, GBMs can display familiar inheritance. Syndromes that are associated with GBM include Li-Fraumeni, L-2 hydroxyglutaric aciduria, Neurofibromatosis type 1, Ollier/Mafucci, and Turcot. This chapter summarizes the histopathologic features of all major GBM subtypes, as well as includes important clinical features of certain subtypes when relevant. Additionally, the expected histopathological features and subtypes of children, versus adults, versus syndrome-associated will be elucidated. Our goal is to assist the practicing pathologist in recognition and diagnosis of GBM, including intraoperatively, in order to aid neurosurgeons and neuro-oncologists in treatment and patient care decisions.

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Rayi, A., Kobalka, P.J. (2021). Histopathology of Adult and Pediatric Glioblastoma. In: Otero, J.J., Becker, A.P. (eds) Precision Molecular Pathology of Glioblastoma. Molecular Pathology Library. Springer, Cham. https://doi.org/10.1007/978-3-030-69170-7_5

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