- Foreword
- Preface
- Abbreviations
- Contributors
- Chapter 1 The 2016 revision of the WHO classification of tumours of the central nervous system
- Chapter 2 Astrocytic tumours: pilocytic astrocytoma, pleomorphic xanthoastrocytoma, and subependymal giant cell astrocytoma
- Chapter 3 Astrocytic tumours: diffuse astrocytoma, anaplastic astrocytoma, glioblastoma, and gliomatosis cerebri
- Chapter 4 Oligodendroglial tumours
- Chapter 5 Ependymal tumours
- Chapter 6 Choroid plexus tumours
- Chapter 7 Other neuroepithelial tumours: astroblastoma, angiocentric glioma, and chordoid glioma
- Chapter 8 Neuronal and mixed neuronal–glial tumours
- Chapter 9 Embryonal and pineal tumours
- Chapter 10 Tumours of the cranial nerves
- Chapter 11 Meningiomas
- Chapter 12 Other tumours of the meninges
- Chapter 13 Tumours of the haematopoietic system
- Chapter 14 Germ cell tumours
- Chapter 15 Familial tumour syndromes: neurofibromatosis, schwannomatosis, rhabdoid tumour predisposition, Li–Fraumeni syndrome, Turcot syndrome, Gorlin syndrome, and Cowden syndrome
- Chapter 16 Familial tumour syndromes: von Hippel–Lindau disease
- Chapter 17 Familial tumour syndromes: tuberous sclerosis complex
- Chapter 18 Pituitary tumours
- Chapter 19 Metastatic brain tumours
- Chapter 20 Metastatic tumours: spinal cord, plexus, and peripheral nerve
- Chapter 21 Neoplastic meningitis: metastases to the leptomeninges and cerebrospinal fluid
- Index
(p. 65) Other neuroepithelial tumours: astroblastoma, angiocentric glioma, and chordoid glioma
- Chapter:
- (p. 65) Other neuroepithelial tumours: astroblastoma, angiocentric glioma, and chordoid glioma
- Author(s):
Martin J. van den Bent
, Frederic Dhermain
, and Walter Stummer
- DOI:
- 10.1093/med/9780199651870.003.0007
This chapter contains a description of three rare entities: astroblastoma, angiocentric glioma, and chordoid glioma. Because these tumours are so rare, the evidence on how to best treat them is anecdotal and essentially consists of case series, but it is the best guidance available and the presentation of larger series with new cases remain unlikely. If one is confronted with such a case, a meticulous review of the clinical, radiological, and pathological characteristics of the case is indicated, to minimize the risk of an erroneous diagnosis. If the case does not fit in with the descriptions of previous cases, alternative diagnoses should be considered.
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- Foreword
- Preface
- Abbreviations
- Contributors
- Chapter 1 The 2016 revision of the WHO classification of tumours of the central nervous system
- Chapter 2 Astrocytic tumours: pilocytic astrocytoma, pleomorphic xanthoastrocytoma, and subependymal giant cell astrocytoma
- Chapter 3 Astrocytic tumours: diffuse astrocytoma, anaplastic astrocytoma, glioblastoma, and gliomatosis cerebri
- Chapter 4 Oligodendroglial tumours
- Chapter 5 Ependymal tumours
- Chapter 6 Choroid plexus tumours
- Chapter 7 Other neuroepithelial tumours: astroblastoma, angiocentric glioma, and chordoid glioma
- Chapter 8 Neuronal and mixed neuronal–glial tumours
- Chapter 9 Embryonal and pineal tumours
- Chapter 10 Tumours of the cranial nerves
- Chapter 11 Meningiomas
- Chapter 12 Other tumours of the meninges
- Chapter 13 Tumours of the haematopoietic system
- Chapter 14 Germ cell tumours
- Chapter 15 Familial tumour syndromes: neurofibromatosis, schwannomatosis, rhabdoid tumour predisposition, Li–Fraumeni syndrome, Turcot syndrome, Gorlin syndrome, and Cowden syndrome
- Chapter 16 Familial tumour syndromes: von Hippel–Lindau disease
- Chapter 17 Familial tumour syndromes: tuberous sclerosis complex
- Chapter 18 Pituitary tumours
- Chapter 19 Metastatic brain tumours
- Chapter 20 Metastatic tumours: spinal cord, plexus, and peripheral nerve
- Chapter 21 Neoplastic meningitis: metastases to the leptomeninges and cerebrospinal fluid
- Index