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Talk:Central nervous system primitive neuroectodermal tumor

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This is an old revision of this page, as edited by Doc James (talk | contribs) at 02:38, 21 April 2019 (Assessment: WikiProject Medicine: class=C, importance=Mid (assisted)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

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 (article contribs).

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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[reply]

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