Results 11 to 20 of about 19,217 (182)
SPOP and OTUD7A Control EWS–FLI1 Protein Stability to Govern Ewing Sarcoma Growth
Chromosomal translocation results in development of an Ewing sarcoma breakpoint region 1‐Friend leukemia integration 1 (EWS–FLI1) fusion oncogene in the majority of Ewing sarcoma.
Ying Wang +2 more
exaly +2 more sources
Cervical vertebra plana secondary to Ewing sarcoma: A case report [PDF]
Vertebra plana is most commonly associated with Langerhans cell histiocytosis in the pediatric population. However, in extremely rare cases, Ewing sarcoma can also present as vertebra plana in this population. Langerhans cell histiocytosis can present as
Richie Zhang, BA +4 more
doaj +2 more sources
Primary Ewing sarcoma of the kidney: a symptomatic presentation and review of the literature
The objective of this review is to discuss the unique nature of primary renal Ewing sarcoma, including incidence, presentation and management. We also report on a common pattern of presentation, consisting of acute flank pain mimicking a renal stone ...
Jorge L Lockhart, Alejandro R Rodríguez
exaly +2 more sources
Ewing’s Sarcoma Ewing’s sarcoma, an aggressive cancer of bone and soft tissue, primarily affects children and young adults. A t(11;22) translocation is noted in 85 to 90% of cases.
Ludwig, Joseph A. +2 more
openaire +6 more sources
AbstractEwing sarcoma is a rare tumor that requires complex multidisciplinary management. This report describes the general management and standard radiotherapy guidelines in both North America (Children's Oncology Group) and Europe (International Society of Pediatric Oncology).
Bree R. Eaton +6 more
openaire +2 more sources
Extraosseous Ewing sarcoma of the pancreas: a case report [PDF]
Extraosseous Ewing sarcoma is a rare and aggressive malignancy belonging to the Ewing sarcoma family of tumors, primarily affecting soft tissues such as the pelvis, retroperitoneum, and chest wall.
Neslihan Nisa Gecici +3 more
doaj +1 more source
Advances in molecular pathology of Ewing sarcoma [PDF]
Ewing sarcoma is a rare malignant small round cell mesenchymal neoplasm with a characteristic FET family-ETS family fusion gene, and is classified as undifferentiated small round cell sarcoma in the fifth revision of the WHO Classification of Tumors of ...
LIU Hengan, WANG Chaofu
doaj +1 more source
Caregivers Awareness Regarding Health Care offered to their children with Ewing Sarcoma [PDF]
Background: Ewing sarcoma is a very aggressive malignancy tumor that requires complex multidisciplinary management. The aim of the study: Was to assess caregivers’ awareness regarding health care offered to their children with Ewing sarcoma.
Lamyaa Momtaz Mohamed +2 more
doaj +1 more source
Differentially expressed miRNAs in Ewing sarcoma compared to mesenchymal stem cells: low miR-31 expression with effects on proliferation and invasion. [PDF]
Ewing sarcoma, the second most common bone tumor in children and young adults, is an aggressive malignancy with a strong potential to metastasize. Ewing sarcoma is characterised by translocations encoding fusion transcription factors with an EWSR1 ...
Bianca Karnuth +8 more
doaj +1 more source
Bibliometric analysis of Ewing sarcoma from 1993 to 2022
Background Ewing sarcoma has attracted more attention in recent years but has yet to be bibliometrically analyzed. Hence, this study investigated the trend of Ewing sarcoma over the past 30 years with bibliometric analysis.
Guangtao Han, Ting Liu, Pengde Kang
doaj +1 more source

