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PDF The 2021 WHO classification of tumors 5th edition central

DNA methylation profiling and newly recognized tumor types Using a DNA methylation array genome-wide profiling of DNA methylation patterns has become a powerful tool for the diagnosis and classification of CNS tumors particularly those with atypical histology or discordant genetic features [4]

  • What is the classification of CNS tumours in who cns5?

    The classification of CNS tumours in WHO CNS5 follows to a large extent that of WHO 2016; however, the chapter of gliomas and neuronal/neuronal-glial tumours has undergone major revision due to progress in molecular genetics.

  • What does CNS stand for?

    The fifth edition of the WHO Classification of Tumors of the Central Nervous System (CNS), published in 2021, is the sixth version of the international standard for the classification of brain and spinal cord tumors.

  • How has molecular genetics changed the classification of CNS tumours?

    Advances in molecular genetics have resulted in more accurate diagnosis and prognosis of CNS tumours, and this minireview summarises important changes implemented in the last edition of WHO classification of CNS tumours important for the practicing neurosurgeon.

  • What is a CNS grade?

    Tumor grades are now designated specifically as CNS WHO grades 1 –4 ( “CNS ” is always added to distinguish the grading system from those of systemic neoplasms because CNS grading differs conceptually, eg, grading of diffuse astrocytomas from 2 to 4, without a 1). Not Otherwise Specified and Not Elsewhere Classified.

Gliomas, Glioneuronal and Neuronal tumours.

Diffuse gliomas are now divided into those occurring primarily in adults (“adult-type”) or in children (“paediatric type”) (see Table 4). With “primarily” means that paediatric tumours may occur in adults, especially young adults, and adult tumours may rarely appear in children [27]. Adult-type diffuse gliomas now constitute only 3 categories: astr

Embryonal Tumours

Embryonal tumours (listed in Table 7) are all grade 4 and comprise a very heterogenous group of tumours with regard to histopathology and molecular genetics. They predominate amongst children and young adults. The term “primitive neuroectodermal tumour”, previously used to include many of these tumours, is outmoded due to progress in molecular gene

Cranial and Paraspinal Nerve Tumours

Cranial and paraspinal nerve tumours (shown in Table 8) may arise sporadically or in a setting of tumour predisposition syndromes, such as neurofibromatosis type 1 and 2 (NF1/2). In case of NF1, there is a proposed nomenclature for the spectrum of the related nerve tumours. Amongst schwannomas and neurofibromas, there are some subtypes; amongst the

Meningiomas

Histopathological grading is a strong prognostic factor in human meningiomas and is important for therapeutic strategies and follow-up regimes [15]. The grading system in WHO CNS5 is comparable with WHO 2016 with three malignancy grades (CNS WHO grades 1–3) based on histopathology or subtype (Table 9). Meningiomas are now regarded as a single tumou

Mesenchymal, Non-Meningothelial Tumours

These mesenchymal tumours are principally similar to those elsewhere in the body, and the nomenclature and histopathology of these tumours now harmonise more with the WHO classification of bone and soft tissue tumours [44]. In general, these tumours are rare in CNS, and in the revised classification, only those unique of CNS are enrolled (see Table

Haematolymphoid Tumours

Lymphomas and histiocytic tumours are now grouped together and include those most common in CNS. Lymphomas may occur in all organs. It is therefore important to distinguish between primary and secondary manifestation of the CNS. The classification of these tumours is in line with WHO 2016. Most common primary CNS lymphoma is diffuse large B-cell ly

Tumours of The Sellar Region

In WHO CNS5, adamantinomatous and papillary craniopharyngiomas are regarded as separate and distinct tumour types. Pituitary adenomas are diagnosed in accordance with the guidelines of WHO Blue Book of Endocrine Tumours [32]. link.springer.com

Metastases

Metastatic tumours to CNS are divided into those that involve brain and spinal cord parenchyma and the meninges. Regarding the latter, terms like “leptomeningeal cancer”, “neoplastic meningitis” and “(lepto)meningeal carcinomatosis” are not recommended. link.springer.com

Genetic Tumour Syndromes of The CNS

The advent of molecular genetics has increased our knowledge of genetic tumour syndromes, so in the last WHO edition new entities are added. It is important to be aware of these syndromes, especially because of specific tumour types, clinical course and therapeutic consequences. link.springer.com

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