Results 1 to 10 of about 18,467 (180)
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
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High‐Dose Continuous Infusion Ifosfamide as Effective Palliation in a Patient With Relapsed Ewing Sarcoma With Bone Marrow Infiltration and Severe Thrombocytopenia: A Case Report [PDF]
Background Ewing sarcoma is a rare primary mesenchymal tumor of the bone that requires an intensive multimodal therapeutic approach. Multidrug chemotherapy regimens are also the backbone for relapsing/recurring Ewing sarcoma treatment, yet when the ...
Fabio Murtas +11 more
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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
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Ewing sarcoma is the second most frequently occurring malignant tumor of the bone and soft tissue in adolescents and young adults. Genetically, Ewing sarcoma is characterized by balanced chromosomal translocation in which a member of FET gene family is ...
Hee Young Ju
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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
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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
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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
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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
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Ewing sarcoma genomics and recent therapeutic advancements
Ewing sarcomas are highly heterogenous mesenchymal tumors that develop in bone or soft tissue and primarily affect children, teenagers, and young adults. After osteosarcoma, it is the second most common malignant bone sarcoma.
Manisha Chavan +6 more
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