Results 161 to 170 of about 19,295 (207)
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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
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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
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Abstract: Ewing sarcoma (ES) is the second most common primary musculoskeletal neoplasm in children and adolescents after osteosarcoma with a peak between 10 and 20. Rarely, the tumor develops in newborns or in adults over the age of 30. ES can affect either the appendicular or axial skeleton. Extraosseous ES is less prevalent. Clinical presentation is
Vanhoenacker, Filip M. +3 more
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Vanhoenacker, Filip M. +3 more
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Ewing's sarcoma of the mandible
Oral Surgery, Oral Medicine, Oral Pathology, 1977Ewing's sarcoma of the head and neck, particularly of the mandible, has a low incidence of occurrence (fifty-five cases in the literature). The present case report demonstrates well the clinical, diagnostic, and therapeutic features in a patient treated at the Head and Neck Service of the Fundação Antonio Prudente, São Paulo, Brazil.
A, Rapoport +5 more
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Retroperitoneal Ewing’s Sarcoma
Urologia Internationalis, 2010We 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 micrograph and immunohistochemical staining using a newly developed mouse monoclonal antibody 5C11, which ...
M, Oya +5 more
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Ewings’ sarcoma of the mandible
The Journal of Laryngology & Otology, 2003Ewings’ sarcoma involving the facial bones is rare although it is the second most frequent bone malignancy. For the diagnosis a biopsy is needed. Currently the treatment is the combination of chemotherapy and radiotherapy with surgery indicated in only a few instances.
Juan L, Quesada +3 more
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Future Oncology, 2010
Although Ewing sarcoma represents a rare malignancy of childhood and adolescence, it has attracted the attention of an increasing number of excellent researchers. With a tumor-specific EWS-ETS translocation coding for a transcription factor, which obviously profoundly modifies the intracellular signaling network, this rare malignancy opens insights in ...
Uta, Dirksen, Heribert, Jürgens
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Although Ewing sarcoma represents a rare malignancy of childhood and adolescence, it has attracted the attention of an increasing number of excellent researchers. With a tumor-specific EWS-ETS translocation coding for a transcription factor, which obviously profoundly modifies the intracellular signaling network, this rare malignancy opens insights in ...
Uta, Dirksen, Heribert, Jürgens
openaire +2 more sources