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Difference between revisions of "Soft tissue lesions"
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→Extrarenal malignant rhabdoid tumour
(→Extrarenal malignant rhabdoid tumour: more ihc) |
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*Essentially identical to ''[[renal malignant rhabdoid tumour]]''.<ref name=Ref_WMSP627>{{Ref WMSP|627}}</ref> | *Essentially identical to ''[[renal malignant rhabdoid tumour]]''.<ref name=Ref_WMSP627>{{Ref WMSP|627}}</ref> | ||
===General=== | ===General=== | ||
* | *Usually children < 2 years old. | ||
*Very poor prognosis. | *Very poor prognosis ~ mean survival in one series 9 months.<ref name=pmid25085603>{{Cite journal | last1 = Uwineza | first1 = A. | last2 = Gill | first2 = H. | last3 = Buckley | first3 = P. | last4 = Owens | first4 = C. | last5 = Capra | first5 = M. | last6 = O'Sullivan | first6 = C. | last7 = McDermott | first7 = M. | last8 = Brett | first8 = F. | last9 = Farrell | first9 = M. | title = Rhabdoid tumor: the Irish experience 1986-2013. | journal = Cancer Genet | volume = 207 | issue = 9 | pages = 398-402 | month = Sep | year = 2014 | doi = 10.1016/j.cancergen.2014.05.015 | PMID = 25085603 }}</ref> | ||
*In the CNS it is known as ''[[atypical teratoid-rhabdoid tumour]]''.<ref name=Ref_WMSP627>{{Ref WMSP|627}}</ref> | *In the CNS it is known as ''[[atypical teratoid-rhabdoid tumour]]''.<ref name=Ref_WMSP627>{{Ref WMSP|627}}</ref> | ||