Atypical teratoid rhabdoid tumor classification: Difference between revisions

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Revision as of 21:27, 14 December 2015

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

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 __NOTOC__
 {{Atypical teratoid rhabdoid tumor}}
-{{CMG}}
+{{CMG}}{{AE}}{{SR}}
+==Overview==
 ==Classification==
-* Primary
-* 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==
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 [[Category:Pediatric cancers]]
 [[Category:Disease]]
-[[Category:Needs overview]]
+[[Category:Overview]]