Neuro-imaging of glioneuronal tumors

Benjamin P. Liu; Rujman U. Zaman; Michelle J. Naidich; Karan S. Dixit

doi:10.1016/B978-0-12-822835-7.00031-7

Neuro-imaging of glioneuronal tumors

Benjamin P. Liu, Rujman U. Zaman, Michelle J. Naidich, Karan S. Dixit

Research output: Chapter in Book/Report/Conference proceeding › Chapter

1 Scopus citations

Abstract

Glioneuronal tumours are rare primary brain tumours composed of both glial and neuronal elements. In most cases, they are benign tumours that are often cured with surgical resection alone. Radiation therapy is sometimes used to treat residual or aggressive tumours. The role of chemotherapy for these tumors is not well defined or is not indicated in most cases. Recently identified molecular markers offer the potential for targeted therapy and personalized medicine. This chapter reviews the available literature on these rare tumours and describes the diagnosis, treatment, and prognosis of each tumour subtype.

Original language	English (US)
Title of host publication	Handbook of Neuro-Oncology Neuroimaging
Publisher	Elsevier
Pages	681-703
Number of pages	23
ISBN (Electronic)	9780128228357
ISBN (Print)	9780128229958
DOIs	https://doi.org/10.1016/B978-0-12-822835-7.00031-7
State	Published - Jan 1 2022

Keywords

Brain tumour
Desmoplastic infantile astrocytoma (DIA)
Desmoplastic infantile ganglioglioma (DIG)
Diffuse leptomeningeal glioneuronal tumour
Dysembroplastic neuroepithelial tumour
Gangliocytoma
Ganglioglioma
Lhermitte–Duclos
Liponeurocytoma
Multi-nodular and vacuolating neuronal tumour
Myxoid glioneuronal tumour
Neurocytoma
Neuronal tumours
PLNTY
Papillary glioneuronal tumour
Paraganglioma
Rosette-forming glioneuronal tumour

ASJC Scopus subject areas

General Medicine

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10.1016/B978-0-12-822835-7.00031-7

Cite this

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title = "Neuro-imaging of glioneuronal tumors",

abstract = "Glioneuronal tumours are rare primary brain tumours composed of both glial and neuronal elements. In most cases, they are benign tumours that are often cured with surgical resection alone. Radiation therapy is sometimes used to treat residual or aggressive tumours. The role of chemotherapy for these tumors is not well defined or is not indicated in most cases. Recently identified molecular markers offer the potential for targeted therapy and personalized medicine. This chapter reviews the available literature on these rare tumours and describes the diagnosis, treatment, and prognosis of each tumour subtype.",

keywords = "Brain tumour, Desmoplastic infantile astrocytoma (DIA), Desmoplastic infantile ganglioglioma (DIG), Diffuse leptomeningeal glioneuronal tumour, Dysembroplastic neuroepithelial tumour, Gangliocytoma, Ganglioglioma, Lhermitte–Duclos, Liponeurocytoma, Multi-nodular and vacuolating neuronal tumour, Myxoid glioneuronal tumour, Neurocytoma, Neuronal tumours, PLNTY, Papillary glioneuronal tumour, Paraganglioma, Rosette-forming glioneuronal tumour",

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AU - Naidich, Michelle J.

AU - Dixit, Karan S.

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N2 - Glioneuronal tumours are rare primary brain tumours composed of both glial and neuronal elements. In most cases, they are benign tumours that are often cured with surgical resection alone. Radiation therapy is sometimes used to treat residual or aggressive tumours. The role of chemotherapy for these tumors is not well defined or is not indicated in most cases. Recently identified molecular markers offer the potential for targeted therapy and personalized medicine. This chapter reviews the available literature on these rare tumours and describes the diagnosis, treatment, and prognosis of each tumour subtype.

AB - Glioneuronal tumours are rare primary brain tumours composed of both glial and neuronal elements. In most cases, they are benign tumours that are often cured with surgical resection alone. Radiation therapy is sometimes used to treat residual or aggressive tumours. The role of chemotherapy for these tumors is not well defined or is not indicated in most cases. Recently identified molecular markers offer the potential for targeted therapy and personalized medicine. This chapter reviews the available literature on these rare tumours and describes the diagnosis, treatment, and prognosis of each tumour subtype.

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KW - Desmoplastic infantile astrocytoma (DIA)

KW - Desmoplastic infantile ganglioglioma (DIG)

KW - Diffuse leptomeningeal glioneuronal tumour

KW - Dysembroplastic neuroepithelial tumour

KW - Gangliocytoma

KW - Ganglioglioma

KW - Lhermitte–Duclos

KW - Liponeurocytoma

KW - Multi-nodular and vacuolating neuronal tumour

KW - Myxoid glioneuronal tumour

KW - Neurocytoma

KW - Neuronal tumours

KW - PLNTY

KW - Papillary glioneuronal tumour

KW - Paraganglioma

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BT - Handbook of Neuro-Oncology Neuroimaging

PB - Elsevier

ER -

Neuro-imaging of glioneuronal tumors

Abstract

Keywords

ASJC Scopus subject areas

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