Abstract
The term ganglioglioma was first coined by Perkins in 1926 to refer to an intracranial tumor composed of both neoplastic astrocytes and atypical ganglion cells. Gangliogliomas were then described by Cushing in his monograph published in 1927 and by Courville in 1930, who provided the first review published on 20 cases [24]. According to subsequent reports, these tumors accounted for an incidence of 0.3–0.97% of all central nervous system (CNS) tumors [10, 24]. Recent studies, however, suggest that gangliogliomas are not as uncommon as previously thought. With the more extensive use of magnetic resonance imaging (MRI) and improved sensitivity and accuracy of histological diagnosis, the incidence of gangliogliomas is actually believed to range between 1.3% and 10% of all primary central nervous system neoplasms [10, 22]. They are more frequently found in children and young adults with a mean age ranging from 8.5 to 31 years, 60–80% of the patients being less than 30 years old [22]. There is a slight male preponderance in most series, though many authors report an almost equal distribution between the two sexes [7].
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Rocco, C.D., Tamburrini, G. (2010). Ganglioglioma. In: Tonn, JC., Westphal, M., Rutka, J.T. (eds) Oncology of CNS Tumors. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-02874-8_27
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DOI: https://doi.org/10.1007/978-3-642-02874-8_27
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