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2007 WHO Classification
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World Health Organization Classification of Tumors of the Central Nervous System
From:
Louis DN, Ohgaki H, Wiestler OD, Cavenee WK (eds) (2007) 
World Health Organization Classification of Tumours of the Central Nervous System.
IARC, Lyon

As cited in:
Louis DN, Ohgaki H, Wiestler OD, Cavenee WK, Burger PC, Jouvet A, Scheithauer BW, Kleihues P
The 2007 WHO Classification of Tumours of the Central Nervous System
Acta Neuropathol (2007) 114:97-109


Contents



Tumors of Neuroepithelial Tissue

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Astrocytic Tumors
1 9421/1(*) Pilocytic Astrocytoma WHO grade I
9425/3(**) Pilomyxoid Astrocytoma WHO grade II
2 9384/1 Subependymal Giant Cell Astrocytoma WHO grade I
3 9424/3 Pleomorphic Xanthoastrocytoma WHO grade II
4 9400/3 Diffuse Astrocytoma WHO grade II
9420/3 Fibrillary Astrocytoma
9411/3 Gemistocytic Astrocytoma
9410/3 Protoplasmatic Astrocytoma
5 9401/3 Anaplastic Astrocytoma WHO grade III
6 9440/3 Glioblastoma WHO grade IV
9441/3 Giant Cell Glioblastoma WHO grade IV
9442/3 Gliosarcoma WHO grade IV
7 9381/3 Gliomatosis Cerebri



Oligodendroglial Tumors
8 9450/3 Oligodendroglioma WHO grade II
9 9451/3 Anaplastic Oligodendroglioma WHO grade III



Oligoastrocytic Tumors
10 9382/3 Oligoastrocytoma WHO grade II
11 9382/3 Anaplastic Oligoastrocytoma WHO grade III



Ependymal Tumors
12 9383/1 Subependymoma WHO grade I
13 9394/1 Myxopapillary Ependymoma WHO grade I
14 9391/3 Ependymoma WHO grade II
9391/3 Cellurar
9393/3 Papillary
9391/3 Clear Cell
9391/3 Tanycytic
15 9392/3 Anaplastic Ependymoma WHO grade III



Choroid Plexus Tumors
16 9390/0 Choroid Plexus Papilloma WHO grade I
17 9390/1 Atypical Choroid Plexus Papilloma WHO grade II
18 9390/3 Choroid Plexus Carcinoma WHO grade III



Other Neuroepithelial Tumors
19 9430/3 Astroblastoma WHO grade I
20 9444/1 Chordoid Glioma of the Third Ventricle WHO grade II
21 9431/1 Angiocentric Glioma WHO grade I



Neuronal and Mixed Neuronal-Glial Tumors
22 9493/0 Dysplastic Gangliocytoma of Cerebellum (Lhermitte-Duclos)
23 9412/1 Desmoplastic Infantile Astrocytoma / Ganglioglioma WHO grade I
24 9413/0 Dysembryoplastic Neuroepithelial Tumor WHO grade I
25 9492/0 Gangliocytoma WHO grade I
26 9505/1 Ganglioglioma WHO grade I
27 9505/3 Anaplastic Ganglioglioma WHO grade III
28 9506/1 Central Neurocytoma WHO grade II
29 9506/1 Extraventricular Neurocytoma WHO grade II
30 9506/1 Cerebellar Liponeurocytoma WHO grade II
31 9509/1 Papillary Glioneuronal Tumor WHO grade I
32 9509/1 Rosette-forming Glioneuronal T. of the Fouth Ventricle WHO grade I
33 8680/1 Paraganglioma WHO grade I



Tumors of the Pineal Region
34 9361/1 Pineocytoma WHO grade I
35 9362/3 Pineal Parenchymal T. of Intermediate Differentiation WHO grade II, III
36 9362/3 Pineoblastoma WHO grade IV
37 9395/3 Papillary Tumor of the Pineal Region WHO grade II, III



Embryonal Tumors
38 9470/3 Medulloblastoma WHO grade IV
9471/3 Desmoplastic/Nodular Medulloblastoma
9471/3 Medulloblastoma with Extensive Nodularity
9474/3 Anaplastic Medulloblastoma
9474/3 Large Cell Medulloblastoma
39 9473/3 CNS Primitive Neuroectodermal Tumor WHO grade IV
9500/3 CNS Neuroblastoma
9490/3 CNS Ganglioneuroblastoma
9501/3 Medulloepithelioma
9392/3 Ependymoblastoma
40 9508/3 Atypical Teratoid/Rhabdoid Tumor WHO grade IV


Tumors of Cranial and Paraspinal Nerves

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41 9560/0 Schwannoma (Neurilemmoma, Neurinoma) WHO grade I
9560/0 Cellular
9560/0 Plexiform
9560/0 Melanotic



42 9540/0 Neurofibroma WHO grade I
9550/0 Plexiform



43 Perineurioma WHO grade I, II, III
9571/0 Perineurioma, NOS
9571/3 Malignant Perineurioma



44 Malignant Peripheral Nerve Sheath Tumor (MPNST) WHO grade II, III, IV
9540/3 Epithelioid MPNST
9540/3 MPNST with Mesenchymal Differentiation
9540/3 Melanotic MPNST
9540/3 MPNST with Glandular Differentiation


Tumors of the Meninges

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Tumors of Meningothelial Cells
45 9530/0 Meningioma WHO grade I
9531/0 Meningothelial
9532/0 Fibrous (Fibroblastic)
9537/0 Transitional (Mixed)
9533/0 Psammomatous
9534/0 Angiomatous
9530/0 Microcystic
9530/0 Secretory
9530/0 Lymphoplasmacyte-rich
9530/0 Metaplastic
9538/1 Chordoid
9538/1 Clear Cell
9539/1 Atypical WHO grade II
9538/3 Papillary
9538/3 Rhabdoid
9530/3 Anaplastic (Malignant) WHO grade III



Mesenchymal Tumors
46 8850/0 Lipoma
47 8861/0 Angiolipoma
48 8880/0 Hibernoma
49 8850/3 Liposarcoma
50 8815/0 Solitary Fibrous Tumor
51 8810/3 Fibrosarcoma
52 8830/3 Malignant Fibrous Histiocytoma
53 8890/0 Leiomyoma
54 8890/3 Leiomyosarcoma
55 8900/0 Rhabdomyoma
56 8900/3 Rhabdomyosarcoma
57 9220/0 Chondroma
58 9220/3 Chondrosarcoma
59 9180/0 Osteoma
60 9180/3 Osteosarcoma
61 9210/0 Osteochondroma
62 9120/0 Haemangioma
63 9133/1 Epithelioid Haemangioendothelioma
64 9150/1 Haemangiopericytoma WHO grade II
65 9150/3 Anaplastic Haemangiopericytoma WHO grade III
66 9120/3 Angiosarcoma
67 9140/3 Kaposi Sarcoma
68 9364/3 Ewing Sarcoma - PNET



Primary Melanocytic Lesions
69 8728/0 Diffuse Melanocytosis
70 8728/1 Melanocytoma
71 8720/3 Malignant Melanoma
72 8728/3 Meningeal Melanomatosis



Other Neoplasms Related to the Meninges
73 9161/1 Haemangioblastoma WHO grade I


Tumors of the Haematopoietic System

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74 9590/3 Malignant Lymphomas
75 9731/3 Plasmacytoma
76 9930/3 Granulocytic Sarcoma


Germ Cell Tumors

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77 9064/3 Germinoma
78 9070/3 Embryonal Carcinoma
79 9071/3 Yolk Sac Tumor
80 9100/3 Choriocarcinoma
81 9080/1 Teratoma
9080/0 Mature
9080/3 Immature
9084/3 Teratoma with Malignant Transformation
82 9085/3 Mixed Germ Cell Tumors


Tumors of the Sellar Region

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83 9350/1 Craniopharyngioma WHO grade I
9351/1 Adamantinomatous
9352/1 Papillary
84 9582/0 Granular Cell Tumor WHO grade I
85 9432/1 Pituicytoma WHO grade I
86 8991/0 Spindle Cell Oncocytoma of the Adenohypophysis WHO grade I


Metastatic Tumors

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Notes

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(*) Morphology code of the International Classification of Diseases for Oncology (ICD-O) {614A} and the Systematized Nomenclature of Medicine (http://snomed.org). Behaviour is coded /0 for benign tumors, /3 for malignant tumors and /1 for borderline or uncertain behaviour.
(**) The italicised numbers are provisional codes proposed for the 4th edition of ICD-O. While they are expected to be incorporated into the next ICD-O edition, they currently remain subject to change.

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