Warning

This consensus document is not a rigid constraint on clinical practice, but a concept of good practice against which the needs of the individual patient should be considered. It therefore remains the responsibility of the individual clinician to interpret the application of these guidelines, taking into account local service constraints and the needs and wishes of the patient. It is not intended that these consensus documents are applied as rigid clinical protocols. 

Principles 

  • To provide a standard approach to the diagnosis of adult glioma across Scotland, using WHO Classification of Tumours of the Central Nervous System4 
  • To work to RCPath Standards and datasets for reporting cancers: Dataset for histopathological reporting of tumours of the central nervous system in adults, including the pituitary gland1
  • To deliver histological diagnosis initially, with a final integrated molecular pathology report within 21 days of surgery  

Who reports CNS tumours

For the purposes of reporting CNS tumours, the NICE guidance on Improving outcomes for people with brain and other CNS tumours defines a neuropathologist as “an accredited pathologist who is registered as a neuropathologist or histopathologist, has specialist expertise in neuro- oncology, and takes part in the national External Quality Assurance (EQA) scheme for neuropathology organised by the British Neuropathological Society”. NICE guidelines also emphasise the central role of the MDT meeting in the management of CNS tumours.Pathologists reporting CNS tumours should attend these meetings and participate in the relevant EQA scheme. 

Clinical information required on the specimen request form

Clinical details, as provided by the submitting clinician on the request form, should be recorded on the pathology report. Relevant clinical history is essential to provide adequate interpretation of the histological findings. We recommend following ICCR Tumours of the Central Nervous System Histological Assessment Reporting Guidethis includes location and focality of the tumour, neuroimaging findings, previous diagnoses and therapies.

Macroscopic assessment

This should include dimensions of the specimens provided, and detail any intra-operative diagnosis offered at the time of surgery. If possible, a fresh frozen sample should be retained for molecular diagnostics.

Histopathological assessment

This should include a detailed microscopic description of the tumour including WHO CNS Grade4.

Molecular analysis

Figure 1 shows an algorithm applied in the diagnosis of an adult glioma, and this should be undertaken for all cases as required. Additional molecular diagnostics, such as methylation profiling, RNA fusion panels, and DNA WGS, should be available for cases as required. 

Figure 1: Diagnostic algorithm for glioma diagnosis5.

Integrated report

A final integrated report incorporating histopathological diagnosis and molecular diagnosis should be issued, in line with WHO Classification of Tumours of the Central Nervous System 4.

Multidisciplinary team (MDT) meeting

A neuropathologist should present all cases at the MDT. 

Audit

All departments issuing integrated neuropathology reports should show evidence of internal audit in relation to diagnostics, and regular audit activities to review compliance with published standards. All consultants must undertake relevant CPD, and successfully complete appraisal annually. 

Editorial Information

Last reviewed: 20/09/2022

Next review date: 20/09/2026

Author(s): Colin Smith on behalf of the Neuropathology Subgroup.

Version: 1

Reviewer name(s): Noelle O'Rourke.