Central Nervous System Tumours Who Classification of Tumours 5th Edition by Who Classification Of Tumours Editorial Board ISBN 978-9283245087 9283245083

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ISBN 10: 9283245083

ISBN 13:  978-9283245087

Author: Who Classification Of Tumours Editorial Board
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The WHO Classification of Tumours

Central Nervous System Tumours is the sixth volume in the 5th edition of the WHO series on the classification of human tumors. This series (also known as the WHO Blue Books) is regarded as the gold standard for the diagnosis of tumors and comprises a unique synthesis of histopathological diagnosis with digital and molecular pathology. These authoritative and concise reference books provide indispensable international standards for anyone involved in the care of patients with cancer or in cancer research, underpinning individual patient treatment as well as research into all aspects of cancer causation, prevention, therapy, and education.

What’s new in this edition?

The 5th edition, guided by the WHO Classification of Tumours Editorial Board, will establish a single coherent cancer classification presented across a collection of individual volumes organized on the basis of anatomical site (digestive system, breast, soft tissue and bone, etc.) and structured in a systematic manner, with each tumor type listed within a taxonomic classification: site, category, family (class), type, and subtype. In each volume, the entities are now listed from benign to malignant and are described under an updated set of headings, including histopathology, diagnostic molecular pathology, staging, and easy-to-read essential and desirable diagnostic criteria.

Who should read this book?

• Pathologists
• Neuro-oncologists
• Neuroradiologists
• Medical oncologists
• Radiation oncologists
• Neurosurgeons
• Oncology nurses
• Cancer researchers
• Epidemiologists
• Cancer registrars

This volume

• Prepared by 199 authors and editors
• Contributors from around the world
• More than 1100 high-quality images
• More than 3600 references

WHO Classification of Tumours Online

• The content of this renowned classification series is now also available in a convenient digital format by purchasing a subscription directly from IARC

Table of contents: 

1. List of Abbreviations

2. Ependymal Tumours

3. Introduction

4. Foreword

5. Supratentorial Ependymoma

6. Supratentorial Ependymoma, ZFTA Fusion-Positive

7. ICD-O Topographical Coding

8. Supratentorial Ependymoma, YAP1 Fusion-Positive

9. Posterior Fossa Ependymoma

10. ICD-O Morphological Coding

11. Posterior Fossa Group A (PFA) Ependymoma

12. CNS Tumours

13. Posterior Fossa Group B (PFB) Ependymoma

14. Spinal Ependymoma

15. Introduction to CNS Tumours

16. Spinal Ependymoma, MYCN-Amplified

17. Myxopapillary Ependymoma

18. Gliomas, Glioneuronal Tumours, and Neuronal Tumours

19. Subependymoma

20. Introduction

21. Adult-Type Diffuse Gliomas

22. Astrocytoma, IDH-Mutant

23. Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted

24. Glioblastoma, IDH-Wildtype

25. Paediatric-Type Diffuse Low-Grade Gliomas

26. Diffuse Astrocytoma, MYB- or MYBL1-Altered

27. Angiocentric Glioma

28. Polymorphous Low-Grade Neuroepithelial Tumour of the Young

29. Diffuse Low-Grade Glioma, MAPK Pathway-Altered

30. Paediatric-Type Diffuse High-Grade Gliomas

31. Diffuse Midline Glioma, H3 K27-Altered

32. Diffuse Hemispheric Glioma, H3 G34-Mutant

33. Diffuse Paediatric-Type High-Grade Glioma, H3-Wildtype and IDH-Wildtype

34. Embryonal Tumours: Introduction

35. Medulloblastomas, Molecularly Defined

36. Medulloblastoma, WNT-Activated

37. Medulloblastoma, SHH-Activated and TP53-Wildtype

38. Medulloblastoma, SHH-Activated and TP53-Mutant

39. Medulloblastoma, Non-WNT/Non-SHH

40. Medulloblastomas, Histologically Defined

41. Other CNS Embryonal Tumours

42. Infant-Type Hemispheric Glioma

43. Circumscribed Astrocytic Gliomas

44. Pilocytic Astrocytoma

45. Atypical Teratoid/Rhabdoid Tumour

46. Cribriform Neuroepithelial Tumour

47. High-Grade Astrocytoma with Piloid Features

48. Pleomorphic Xanthoastrocytoma

49. Subependymal Giant Cell Astrocytoma

50. Chordoid Glioma

51. Embryonal Tumour with Multilayered Rosettes

52. CNS Neuroblastoma, FOXR2-Activated

53. CNS Tumour with BCOR Internal Tandem Duplication

54. CNS Embryonal Tumour NEC/NOS

55. Astroblastoma, MN1-Altered

56. Glioneuronal and Neuronal Tumours

57. Pineal Tumours: Introduction

58. Ganglioglioma

59. Gangliocytoma

60. Pineocytoma

61. Desmoplastic Infantile Ganglioglioma / Desmoplastic Infantile Astrocytoma

62. Pineal Parenchymal Tumour of Intermediate Differentiation

63. Dysembryoplastic Neuroepithelial Tumour

64. Pineoblastoma

65. Diffuse Glioneuronal Tumour with Oligodendroglioma-like Features and Nuclear Clusters

66. Desmoplastic Myxoid Tumour of the Pineal Region, SMARCB1-Mutant

67. Papillary Glioneuronal Tumour

68. Rosette-Forming Glioneuronal Tumour

69. Myxoid Glioneuronal Tumour

70. Diffuse Leptomeningeal Glioneuronal Tumour

71. Multinodular and Vacuolating Neuronal Tumour

72. Dysplastic Cerebellar Gangliocytoma (Lhermitte-Duclos Disease)

73. Central Neurocytoma

74. Extraventricular Neurocytoma

75. Cerebellar Liponeurocytoma

76. Cauda Equina Neuroendocrine Tumour (Paraganglioma)

77. Meningioma

78. Mesenchymal, Non-Meningothelial Tumours Involving the CNS: Introduction

79. Soft Tissue Tumours

80. Fibroblastic and Myofibroblastic Tumours

81. Pituicytoma, Granular Cell Tumour of the Sellar Region, and Spindle Cell Oncocytoma

82. Solitary Fibrous Tumour

83. Vascular Tumours

84. Pituitary Adenoma / Pituitary Neuroendocrine Tumour

85. Haemangiomas and Vascular Malformations

86. Pituitary Blastoma

87. Haemangioblastoma

88. Skeletal Muscle Tumours

89. Rhabdomyosarcoma

90. Tumours of Uncertain Differentiation

91. Metastases to the CNS: Introduction

92. Metastases to the Brain and Spinal Cord Parenchyma

93. Metastases to the Meninges

94. Intracranial Mesenchymal Tumour, FET::CREB Fusion-Positive

95. Genetic Tumour Syndromes Involving the CNS: Introduction

96. Primary Intracranial Sarcoma, DICER1-Mutant

97. Neurofibromatosis Type 1

98. Neurofibromatosis Type 2

99. Schwannomatosis

100. Von Hippel-Lindau Syndrome

101. Tuberous Sclerosis

102. Li-Fraumeni Syndrome

103. Cowden Syndrome

104. Constitutional Mismatch Repair Deficiency Syndrome

105. Familial Adenomatous Polyposis 1

106. Naevoid Basal Cell Carcinoma Syndrome

107. Rhabdoid Tumour Predisposition Syndrome

108. Carney Complex

109. DICER1 Syndrome

110. Familial Paraganglioma Syndromes

111. Melanoma-Astrocytoma Syndrome

112. Familial Retinoblastoma

113. Haematolymphoid Tumours Involving the CNS: Introduction

114. Lymphomas

115. CNS Lymphomas

116. Primary Diffuse Large B-Cell Lymphoma of the CNS

117. Lymphomatoid Granulomatosis

118. Immunodeficiency-Associated CNS Lymphomas

119. Intravascular Large B-Cell Lymphoma

120. Miscellaneous Rare Lymphomas in the CNS

121. MALT Lymphoma of the Dura

122. Other Low-Grade B-Cell Lymphomas of the CNS

123. Anaplastic Large Cell Lymphoma (ALK+/ALK-)

124. T-Cell and NK/T-Cell Lymphomas

125. Histiocytic Tumours

126. Erdheim-Chester Disease

127. Rosai-Dorfman Disease

128. Juvenile Xanthogranuloma

129. Langerhans Cell Histiocytosis

130. Histiocytic Sarcoma

131. Declaration of Interests

132. IARC/WHO Committee for ICD-O

133. Sources

134. References

135. Subject Index

136. Previous Volumes in the Series

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