STBT5:Ewing sarcoma: Difference between revisions
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<nowiki>*</nowiki>Note: These are only the genetic/genomic criteria. Additional diagnostic criteria can be found in the [https://tumourclassification.iarc.who.int/home <u>WHO Classification of Tumours</u>]. | <nowiki>*</nowiki>Note: These are only the genetic/genomic criteria. Additional diagnostic criteria can be found in the [https://tumourclassification.iarc.who.int/home <u>WHO Classification of Tumours</u>]. | ||
==Related Terminology== | ==Related Terminology== | ||
{| class="wikitable" | {| class="wikitable" | ||
|+ | |+ | ||
|Acceptable | |Acceptable | ||
| | |N/A | ||
|- | |- | ||
|Not Recommended | |Not Recommended | ||
| | |Askin tumour (for Ewing sarcoma arising in the chest wall); primitive neuroectodermal tumour | ||
|} | |} | ||
Note: Some small round cell sarcomas previously considered subtypes of Ewing sarcoma (Ewing-like sarcomas) are genetically and clinically distinct entities and include CIC-rearranged sarcoma and sarcoma with BCOR genetic alterations, described in separate sections. | |||
==Gene Rearrangements== | ==Gene Rearrangements== | ||