Ewing's sarcoma

(redirected from Ewing sarcoma)
Also found in: Dictionary, Thesaurus, Medical.
Related to Ewing sarcoma: osteosarcoma

Ewing's sarcoma

[′yü·iŋz sär′kō·mə]
(medicine)
A primary malignant tumor of bone, usually arising as a central tumor in long bone.
References in periodicals archive ?
It is also called, primitive neuroectodermal tumor, Askin tumor (Ewing sarcoma of the chest wall), extraosseous Ewing sarcoma (Ewing sarcoma in tissue other than bone).
In general, precise subclassification would greatly benefit patients with chemosensitive sarcomas, such as synovial sarcoma, Ewing sarcoma, osteosarcoma, rhabdomyosarcoma, desmoplastic small round cell tumor, angiosarcoma, myxoid/round cell liposarcoma, and uterine leiomyosarcoma.
Dion Yates, on the right, is battling Ewing Sarcoma
Successful complete resection of Ewing sarcoma arising from the bladder in a 10-year-old boy after chemotherapy.
The report provides a snapshot of the global therapeutic landscape of Ewing Sarcoma
Ewing sarcoma (ES) and peripheral primitive neuroectodermal tumor (PNET) were originally described as distinct clinicopathologic entities.
Ewing sarcoma of the rib: results of an intergroup study with analysis of outcome by timing of resection.
Therefore, in some rare cases, even if a normal result is reported, a diagnosis of Ewing sarcoma or PNET cannot be completely excluded.
Of the 26 IRG recipients, seven focus significantly on pediatric cancers, including Ewing sarcoma, rhabdoid tumors, and atypical teratoid/rhabdoid tumors (RT).
Massive pleural effusion with dyspnea in a 17-year-old boy as the first sign of ewing sarcoma.
Ewing sarcoma and colon cancer will not benefit from that approach.