Astrocytic tumours

Last revised by Rohit Sharma on 30 Mar 2024

Astrocytic tumours are primary central nervous system tumours that either arises from astrocytes or appear similar to astrocytes on histology having arisen from precursor cells. They are the most common tumours arising from glial cells and can be broadly divided into three groups: 

  1. diffuse, adult-type
  2. diffuse, paediatric type
  3. circumscribed

These can further be divided into individual entities as described in the WHO classification of CNS tumours (5th edition, 2021), many of which are molecularly defined 3

Additionally, some tumours also contain astrocytic components, and it is often this component that dictates biological behaviour. Examples include:

Most of these tumours have strikingly differing demographics, imaging appearances, treatment and prognosis and thus they are, along with spinal astrocytomas discussed separately.

Note: anaplastic astrocytomagliomatosis cerebrifibrillary astrocytoma and protoplasmic astrocytoma, gemistocytic astrocytoma are no longer recognised as distinct entities in the current WHO classification of CNS tumours.

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