Results 191 to 200 of about 82,773 (230)
Ewing's Sarcoma of Mandible: A Case Report with Review of Literature. [PDF]
Int J Clin Pediatr DentBellut N +5 more
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Case Report: Extra skeletal Ewing's sarcoma of mediastinum: clinical experience and literature review. [PDF]
Front OncolHu X, Zhao W, Yu R, Pan D.
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Prognostic factors and overall survival in pelvic Ewing's sarcoma and chordoma: A comparative SEER database analysis. [PDF]
HeliyonTang W, Li R, Lai X, Yu X, He R.
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Ewing's sarcoma family of tumors in adolescents in Beijing 2010-2019: a multicenter retrospective cohort study. [PDF]
Transl PediatrZhao W +12 more
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Ewing's Sarcoma Disguised as Aneurysmal Bone Cyst Lesion: About a Case. [PDF]
Case Rep Oncol MedEl Khassoui A +5 more
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The Lancet Oncology, 2010
Progress in the treatment of Ewing's sarcoma, the second most common bone tumour in children and adolescents, has improved survival from about 10% in the period before chemotherapy was introduced to about 75% today for patients with localised tumours. However, patients with metastases still fare badly, and the therapy carries short-term and long-term ...
Naomi J, Balamuth, Richard B, Womer
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Progress in the treatment of Ewing's sarcoma, the second most common bone tumour in children and adolescents, has improved survival from about 10% in the period before chemotherapy was introduced to about 75% today for patients with localised tumours. However, patients with metastases still fare badly, and the therapy carries short-term and long-term ...
Naomi J, Balamuth, Richard B, Womer
openaire +4 more sources
Radiologic Clinics of North America, 1993
Ewing's sarcoma is a highly malignant tumor of uncertain origin. A strong relationship is suggested between Ewing's sarcoma and tumors of neural origin. The radiologic manifestation of Ewing's sarcoma are protean and lesions may be lytic, mixed lytic-sclerotic, or rarely, predominantly sclerotic.
K D, Eggli, T, Quiogue, R P, Moser
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Ewing's sarcoma is a highly malignant tumor of uncertain origin. A strong relationship is suggested between Ewing's sarcoma and tumors of neural origin. The radiologic manifestation of Ewing's sarcoma are protean and lesions may be lytic, mixed lytic-sclerotic, or rarely, predominantly sclerotic.
K D, Eggli, T, Quiogue, R P, Moser
openaire +4 more sources
Seminars in Diagnostic Pathology, 2014
Classification of small round cell tumors of bone is often challenging due to overlapping clinicopathologic features. The purpose of this article is to review the clinical, radiological, histologic, and molecular features of Ewing sarcoma and to provide a discussion of the differential diagnosis of small round cell tumors of bone.
Eun-Young K, Choi +4 more
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Classification of small round cell tumors of bone is often challenging due to overlapping clinicopathologic features. The purpose of this article is to review the clinical, radiological, histologic, and molecular features of Ewing sarcoma and to provide a discussion of the differential diagnosis of small round cell tumors of bone.
Eun-Young K, Choi +4 more
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Nature Reviews Disease Primers, 2018
Ewing sarcoma is the second most frequent bone tumour of childhood and adolescence that can also arise in soft tissue. Ewing sarcoma is a highly aggressive cancer, with a survival of 70-80% for patients with standard-risk and localized disease and ~30% for those with metastatic disease.
Grünewald, Thomas G. P. +8 more
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Ewing sarcoma is the second most frequent bone tumour of childhood and adolescence that can also arise in soft tissue. Ewing sarcoma is a highly aggressive cancer, with a survival of 70-80% for patients with standard-risk and localized disease and ~30% for those with metastatic disease.
Grünewald, Thomas G. P. +8 more
openaire +6 more sources