Atypical teratoid rhabdoid tumor classification: Difference between revisions

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Latest revision as of 19:11, 14 May 2019

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sujit Routray, M.D. [2]

There is no classification system established for atypical teratoid rhabdoid tumor.

There is no classification system established for atypical teratoid rhabdoid tumor.^[1]

↑ Classification of atypical teratoid rhabdoid tumor. Dana-Farber Cancer Institute 2015. http://www.dana-farber.org/Health-Library/Childhood-AT/RT---Atypical-Teratoid-Rhabdoid-Tumor.aspx. Accessed on December 14, 2015

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 __NOTOC__
 {{Atypical teratoid rhabdoid tumor}}
-{{CMG}}
+{{CMG}}{{AE}}{{SR}}
 ==Overview==
+There is no [[classification]] system established for atypical teratoid rhabdoid tumor.
 ==Classification==
-* Primary
+There is no [[classification]] system established for atypical teratoid rhabdoid tumor.<ref name="classatrt1">Classification of atypical teratoid rhabdoid tumor. Dana-Farber Cancer Institute 2015. http://www.dana-farber.org/Health-Library/Childhood-AT/RT---Atypical-Teratoid-Rhabdoid-Tumor.aspx. Accessed on December 14, 2015</ref>
-* Secondary
-AT/RT may be related to [[rhabdoid tumour|malignant rhabdoid tumor]] (MRT), which occurs outside the CNS, usually in the kidney. The finding that AT/RT and MRT both have deletions of the INI1 gene indicates that rhabdoid tumors of the kidney and brain are at least closely related. AT/RT and MRT also have similar [[histology]] and similar clinical and demographic features. Moreover, 10–15% of MRT patients have simultaneous or subsequent brain tumors, many of which are secondary or primary MRT.
+==References==
+{{reflist|1}}
-==References==
-{{reflist|2}}
-{{WH}}
-{{WS}}
-[[Category:Oncology]]
 [[Category:Types of cancer]]
 [[Category:Rare cancers]]
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 [[Category:Pediatric cancers]]
 [[Category:Disease]]
+[[Category:Oncology]]
+{{WH}}
+{{WS}}