Results 131 to 140 of about 5,957 (165)
A prognostic model correlated with fatty acid metabolism in Ewing's sarcoma based on bioinformatics analysis. [PDF]
Open Med (Wars)Chen X +7 more
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Metastatic extension of Ewing's sarcoma to the right heart chambers: a rare case report. [PDF]
Egypt Heart JEttagmouti Y +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
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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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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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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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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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Journal of Hand Surgery (European Volume), 2008
A retrospective case review was carried out to report the outcomes in a contemporary case series of Ewing’s sarcoma originating in the hand. We identified five patients treated since 1995. All five had wide surgical excision, one by ray amputation. All were treated with chemotherapy.
O A, Anakwenze +4 more
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A retrospective case review was carried out to report the outcomes in a contemporary case series of Ewing’s sarcoma originating in the hand. We identified five patients treated since 1995. All five had wide surgical excision, one by ray amputation. All were treated with chemotherapy.
O A, Anakwenze +4 more
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Urology, 2014
Nonosseous Ewing sarcoma commonly occurs in the extremities or deep soft tissues. However, cutaneous and subcutaneous locations have been reported. A 3-year-old boy presented with a 2-year history of a painless, slowly growing mid-scrotal mass. Pathology after surgical excision revealed the lesion to be Ewing sarcoma.
Gwen M, Grimsby, Clanton B, Harrison
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Nonosseous Ewing sarcoma commonly occurs in the extremities or deep soft tissues. However, cutaneous and subcutaneous locations have been reported. A 3-year-old boy presented with a 2-year history of a painless, slowly growing mid-scrotal mass. Pathology after surgical excision revealed the lesion to be Ewing sarcoma.
Gwen M, Grimsby, Clanton B, Harrison
openaire +2 more sources