WHO classification of tumours of the central nervous system

MRI of a patient with anaplastic astrocytoma

The following is a simplified (deprecated) version of the 2021 WHO classification of the tumours of the central nervous system. Currently, as of 2021, clinicians are using the WHO grade 5th edition, which incorporates recent advances in molecular pathology.

Listed for each tumour are the WHO official name, the ICD-O code (with Arabic numeral, where /0 indicates "benign" tumour, /3 malignant tumour and /1 borderline tumour), and the WHO Grade (a parameter connected with the "aggressiveness" of the tumour), also in Arabic numerals as per the updated 2021 guidelines.

1. Gliomas, glioneuronal tumors, and neuronal tumours

1.1 Adult-type diffuse gliomas

1.1.1 Astrocytoma, IDH-mutant

1.1.2 Oligodendroglioma, IDH-mutant, and 1p/19q-codeleted

1.1.3 Glioblastoma, IDH-wildtype

1.2 Pediatric-type diffuse low-grade gliomas

1.2.1 Diffuse astrocytoma, MYB- or MYBL1-altered

1.2.2 Angiocentric glioma

1.2.3 Polymorphous low-grade neuroepithelial tumor of the young (PLNTY)

1.2.4 Diffuse low-grade glioma, MAPK pathway-altered

1.3 Pediatric-type diffuse high-grade gliomas

1.3.1 Diffuse midline glioma, H3 K27-altered

1.3.2 Diffuse hemispheric glioma, H3 G34-mutant

1.3.3 Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype

1.3.4 Infant-type hemispheric glioma

1.4 Circumscribed astrocytic gliomas

1.4.1 Pilocytic astrocytoma

1.4.2 High-grade astrocytoma with piloid features

1.4.3 Pleomorphic xanthoastrocytoma

1.4.4 Subependymal giant cell astrocytoma

1.4.5 Chordoid glioma

1.4.6 Astroblastoma, MN1-altered

1.5 Glioneuronal and neuronal tumours

1.5.1 Ganglioglioma

1.5.2 Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma

1.5.3 Dysembryoplastic neuroepithelial tumor

1.5.4 Diffuse glioneuronal tumor with oligodendroglioma-like features and nuclear clusters

1.5.5 Papillary glioneuronal tumor

1.5.6 Rosette-forming glioneuronal tumor

1.5.7 Myxoid glioneuronal tumor

1.5.8 Diffuse leptomeningeal glioneuronal tumor

1.5.9 Gangliocytoma

1.5.10 Multinodular and vacuolating neuronal tumor

1.5.11 Dysplastic cerebellar gangliocytoma (Lhermitte-Duclos disease)

1.5.12 Central neurocytoma

1.5.13 Extraventricular neurocytoma

1.5.14 Cerebellar liponeurocytoma

1.6 Ependymal tumours

1.6.1 Supratentorial ependymoma

1.6.1.1 Supratentorial ependymoma, ZFTA fusion-positive

1.6.1.2 Supratentorial ependymoma, YAP1 fusion-positive

1.6.2 Posterior fossa ependymoma

1.6.2.1 Posterior fossa ependymoma, group PFA

1.6.2.2 Posterior fossa ependymoma, group PFB

1.6.3 Spinal ependymoma

1.6.3.1 Spinal ependymoma, MYCN-amplified

1.6.4 Myxopapillary ependymoma

1.6.5 Subependymoma

2. Choroid plexus tumours

2.1 Choroid plexus papilloma

2.2 Atypical choroid plexus papilloma

2.3 Choroid plexus carcinoma

3. Embryonal tumours

3.1 Medulloblastoma

3.2 Atypical teratoid/rhabdoid tumour

3.3 Cribiform neuroepithelial tumour

3.4 Embryonal tumour with multilayered rosettes

3.5 CNS neuroblastoma, FOXR2-activated

3.6 CNS tumor with BCOR internal tandem duplication

4. Pineal tumours

4.1 Pineocytoma

4.2 Pineal parenchymal tumour of intermediate differentiation

4.3 Pineoblastoma

4.4 Papillary tumor of the pineal region

4.5 Desmoplastic myxoid tumour of the pineal region, SMARCB1-mutant

5. Cranial and paraspinal nerve tumours

5.1 Schwannoma

5.2 Neurofibroma

5.3 Perineurioma

5.4 Hybrid nerve sheath tumour

5.5 Malignant melanotic nerve sheath tumour

5.6 Malignant peripheral nerve sheath tumour

5.7 Paraganglioma

6. Meningioma

6.1 Meningioma

6.2 Meningothelial meningioma

6.3 Fibrous meningioma

6.4 Transitional meningioma

6.5 Psammomatous meningioma

6.6 Angiomatus meningioma

6.7 Microcystic meningioma

6.8 Secretory meningioma

6.9 Lymphoplasmacyte-rich meningioma

6.10 Metaplastic meningioma

6.11 Chordoid meningioma

6.12 Clear cell meningioma

6.13 Atypical meningioma

6.1 Papillary meningioma

6.1 Rhabdoid meningioma

6.1 Anaplastic (malignant) meningioma

7. Mesenchymal, non-meningothelial tumours

7.1 Soft tissue tumours

7.1.1 Fibroblastic and myofibroblastic tumours

7.1.1.1 Solitary fibrous tumour

7.1.2 Vascular tumours

7.1.2.1 Hemangiomas and vascular malformations

7.1.2.2 Hemangioblastoma

7.1.3 Skeletal muscle tumours

7.1.3.1 Rhabdomyosarcoma

7.1.4 Uncertain differentiation

7.1.4.1 Intracranial mesenchymal tumour, FET-CREB fusion-positive

7.1.4.2 CIC-rearranged sarcoma

7.1.4.3 Primary intracranial sarcoma, DICER1-mutant

7.1.4.4 Ewing sarcoma

7.2 Chondro-osseous tumours

7.2.1 Chondrogenic tumours

7.2.1.1 Mesenchymal chondrosarcoma

7.2.1.2 Chondrosarcoma

7.2.2 Notochordal tumours

7.2.2.1 Chordoma (including poorly differentiated chordoma)

8. Melanocytic tumours

8.1 Diffuse meningeal melanocytic neoplasms

8.1.1 Meningeal melanocytosis and meningeal melanomatosis

8.2 Circumscribed meningeal melanocytic neoplasms

8.2.1 Meningeal melanocytoma and meningeal melanoma

9. Hematolymphoid tumours

9.1 Lymphomas

9.1.1 CNS lymphomas

9.1.1.1 Primary diffuse large B-cell lymphoma of the CNS

9.1.1.2 Immunodeficiency-associated CNS lymphoma

9.1.1.3 Lymphomatoid granulomatosis

9.1.1.4 Intravascular large B-cell lymphoma

9.1.2 Miscellaneous rare lymphomas in the CNS

9.1.2.1 MALT lymphoma of the dura

9.1.2.2 Other low-grade B-cell lymphomas of the CNS

9.1.2.3 Anaplastic large cell lymphoma (ALK+/ALK−)

9.1.2.4 T-cell and NK/T-cell lymphomas

9.2 Histiocytic tumors

9.2.1 Erdheim-Chester disease

9.2.2 Rosai-Dorfman disease

9.2.3 Juvenile xanthogranuloma

9.2.4 Langerhans cell histiocytosis

9.2.5 Histiocytic sarcoma

10. Germ cell tumours

10.1 Mature teratoma

10.2 Immature teratoma

10.3 Teratoma with somatic-type malignancy

10.4 Germinoma

10.5 Embryonal carcinoma

10.6 Yolk sac tumor

10.7 Choriocarcinoma

10.8 Mixed germ cell tumor

11. Tumors of the sellar region

11.1 Adamantinomatous craniopharyngioma

11.2 Papillary craniopharyngioma

11.3 Pituicytoma, granular cell tumor of the sellar region, and spindle cell oncocytoma

11.4 Pituitary adenoma/PitNET

11.5 Pituitary blastoma

12. Metastases to the CNS

12.1 Metastases to the brain and spinal cord parenchyma

12.2 Metastases to the meninges

History

1979 WHO classification (1st edition)

Zülch, Histological typing of tumours of the central nervous system. World Health Organization, Geneva

1993 WHO classification (2nd edition)

reflected the advances brought about by the introduction of immunohistochemistry into diagnostic pathology

Kleihues P, Burger PC, Scheithauer BW (eds) (1993) Histological typing of tumours of the central nervous system. World Health Organization international histological classification of tumours. Springer, Heidelberg

2000 WHO classification (3rd edition)

edited by Kleihues and Cavenee

Kleihues P, Cavenee WK (eds) (2000) World Health Organization Classification of Tumours. Pathology and genetics of tumours of the nervous system. IARC Press

2007 WHO classification (4th edition)

This is the classification that began to suggest the use genetic information for classification.

2016 WHO classification (4th revised edition)

This was a substantial revision of the 4th edition. The reason it is not the 5th edition is that additions to the CNS volume were needed even though WHO was not up to 5th editions yet.

2021 WHO classification (5th edition)

The 5th edition incorporated many of the proposed changes outlined by the cIMPACT-NOW (the Consortium to Inform Molecular and Practical Approaches to CNS Tumor Taxonomy - Not Official WHO).

WHO Classification of Tumours (Online Edition)

Since February 19, 2020, the WHO tumors classification has been accessible online as a subscription service, which includes the revised 4th edition.

See also

• Grading of the tumors of the central nervous system

External links

• AFIP Course Syllabus - Astrocytoma WHO Grading Lecture Handout