Talk:Central nervous system primitive neuroectodermal tumor

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This article provides an elaborate overview of central nervous system primitive neuroectodermal tumor. She has clearly sourced the information from reputable sources that are relevant throughout the article. The lead explains what PNET is like generally, and her sections elaborate on each aspect of the tumor. This tumor is notable in that it has many sources referring to this tumor and recognition from WHO. There are no effective treatments available for this tumor that is normally found in children; the prognosis is not favorable for the patients. Patients tend to survive for less than ten years after diagnosis. The images incorporated in the Wikipedia article allow me to visualize how the tumor looks like. The only thing that I would suggest is that the Risk factors could be divided into subsections such as age and pre-existing genetic conditions.

Beautiful days111 (talk) 04:42, 23 March 2019 (UTC)Beautiful_days111

Wiki Education Foundation-supported course assignment

This article was the subject of a Wiki Education Foundation-supported course assignment, between 8 January 2019 and 16 April 2019. Further details are available on the course page. Student editor(s): Mariarrt.

Above undated message substituted from Template:Dashboard.wikiedu.org assignment by PrimeBOT (talk) 18:49, 17 January 2022 (UTC)

This may be an outdated classification

The 2016 update of the WHO classification of CNS tumors removes the term PNET from the lexicon: "The embryonal tumors other than medulloblastoma have also undergone substantial changes in their classification, with removal of the term primitive neuroectodermal tumor or PNET from the diagnostic lexicon."

Logophile59 (talk) 12:58, 27 April 2019 (UTC)

References