Results 201 to 210 of about 122,719 (232)
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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
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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
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Current Treatment Options in Oncology, 2000
Patients with Ewing's sarcoma should be transferred to a comprehensive cancer center for evaluation and management when the diagnosis is suspected. Proper biopsy technique is essential to preserve all therapeutic options, including limb preservation surgery.
P A, Meyers, A S, Levy
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Patients with Ewing's sarcoma should be transferred to a comprehensive cancer center for evaluation and management when the diagnosis is suspected. Proper biopsy technique is essential to preserve all therapeutic options, including limb preservation surgery.
P A, Meyers, A S, Levy
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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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Oral Surgery, Oral Medicine, Oral Pathology, 1971
Abstract Ewing's sarcoma, a rare neoplasm that usually occurs in persons under 25 years of age, is considered the most lethal of all bone tumors. Treatment usually consists of radiation therapy. Although the value of prophylactic chemotherapy has not been established, encouraging results have been achieved with the use of Cytoxan at periodic ...
W, Carl +3 more
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Abstract Ewing's sarcoma, a rare neoplasm that usually occurs in persons under 25 years of age, is considered the most lethal of all bone tumors. Treatment usually consists of radiation therapy. Although the value of prophylactic chemotherapy has not been established, encouraging results have been achieved with the use of Cytoxan at periodic ...
W, Carl +3 more
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Clinical Radiology, 1971
A study of 244 histologically proven cases of Ewing's Tumour is presented, illustrating its clinical behaviour and radiological appearances. 170 patients were treated between 1941 and 1964 by radiation, surgery, chemotherapy or combinations of these methods. Nine cases survived for more than 5 years.
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A study of 244 histologically proven cases of Ewing's Tumour is presented, illustrating its clinical behaviour and radiological appearances. 170 patients were treated between 1941 and 1964 by radiation, surgery, chemotherapy or combinations of these methods. Nine cases survived for more than 5 years.
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Ewing sarcoma and Ewing-like tumors
Virchows Archiv, 2019Ewing sarcoma (ES) and Ewing-like sarcomas are highly aggressive round cell mesenchymal neoplasms, most often occurring in children and young adults. The identification of novel molecular alterations has greatly contributed to a profound reappraisal of classification, to the extent that the category of undifferentiated round cell sarcoma has ...
Sbaraglia, Marta +3 more
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Pediatric Blood & Cancer, 2005
The occurrence of primary extraosseous Ewing sarcoma (EES) of the central nervous system (CNS) has only rarely been reported in the literature. It is important to distinguish this entity from the more common central primitive neuroectodermal tumor (PNET) of brain, since the management of these tumors is different from that of EES.
Melissa A, Mazur +7 more
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The occurrence of primary extraosseous Ewing sarcoma (EES) of the central nervous system (CNS) has only rarely been reported in the literature. It is important to distinguish this entity from the more common central primitive neuroectodermal tumor (PNET) of brain, since the management of these tumors is different from that of EES.
Melissa A, Mazur +7 more
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Journal of Surgical Oncology, 1983
AbstractA case of Ewings sarcoma arising in the soft tissue of the thumb is described. This appears to be the first case of digital extraskeletal Ewings sarcoma. The soft tissue location, the primary rather than metastatic nature, and the tumor type in this case were well documented.
K T, Chen, A, Padmanabhan
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AbstractA case of Ewings sarcoma arising in the soft tissue of the thumb is described. This appears to be the first case of digital extraskeletal Ewings sarcoma. The soft tissue location, the primary rather than metastatic nature, and the tumor type in this case were well documented.
K T, Chen, A, Padmanabhan
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Retroperitoneal Ewing’s Sarcoma
Urologia Internationalis, 1995We report a case of extraskeletal Ewing's sarcoma arising in the retroperitoneal cavity. The tumor was excised en bloc with the left kidney and infiltrated portion of the left ureter. Histological diagnosis was confirmed by both electron micrography and immunohistochemical staining using a newly developed mouse monoclonal antibody 5C11, which ...
M, Oya +5 more
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