Results 171 to 180 of about 19,295 (207)
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Cancer, 1999
Ewing's sarcoma usually is identified as a primary malignancy of bone affecting children and young adults. Extraskeletal Ewing's sarcoma is rare, and very few data are available addressing optimal surgical and oncologic treatment modalities.The authors chose to review retrospectively 24 patients with extraskeletal Ewing's sarcoma treated at the study ...
R, Ahmad +3 more
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Ewing's sarcoma usually is identified as a primary malignancy of bone affecting children and young adults. Extraskeletal Ewing's sarcoma is rare, and very few data are available addressing optimal surgical and oncologic treatment modalities.The authors chose to review retrospectively 24 patients with extraskeletal Ewing's sarcoma treated at the study ...
R, Ahmad +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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2014
Ewing's sarcoma of bone is a primary bone sarcoma found predominantly in patients during their second decade of life. It is a high-grade aggressive small round blue cell tumor that is part of the Ewing's family of tumors. Its exact eitiology is unknown but it commonly demonstrates reproducible staining of CD99 and translocations of the EWS gene ...
Drew D, Moore, Rex C, Haydon
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Ewing's sarcoma of bone is a primary bone sarcoma found predominantly in patients during their second decade of life. It is a high-grade aggressive small round blue cell tumor that is part of the Ewing's family of tumors. Its exact eitiology is unknown but it commonly demonstrates reproducible staining of CD99 and translocations of the EWS gene ...
Drew D, Moore, Rex C, Haydon
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Journal of Orthopaedic & Sports Physical Therapy, 2018
A 26-year-old active woman with knee pain was seen by her primary care physician and diagnosed with patellofemoral pain (PFP). Radiographs of the knee were interpreted as noncontributory. Her knee symptoms continued, and 8 weeks later she was referred to a physiatrist, who confirmed the PFP diagnosis and referred her to physical therapy.
Katie J, Traver +2 more
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A 26-year-old active woman with knee pain was seen by her primary care physician and diagnosed with patellofemoral pain (PFP). Radiographs of the knee were interpreted as noncontributory. Her knee symptoms continued, and 8 weeks later she was referred to a physiatrist, who confirmed the PFP diagnosis and referred her to physical therapy.
Katie J, Traver +2 more
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Journal of the American Medical Association, 1959
A review of the literature regarding Ewing's sarcoma indicates that tumors located in small bones are apparently a rare finding. In 75% of cases, long bones of the extremities, including the shoulder girdle, were involved; lower extremities were involved in 50% of cases. The predilection for metaphysis in long bones was noted. In the series reported by
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A review of the literature regarding Ewing's sarcoma indicates that tumors located in small bones are apparently a rare finding. In 75% of cases, long bones of the extremities, including the shoulder girdle, were involved; lower extremities were involved in 50% of cases. The predilection for metaphysis in long bones was noted. In the series reported by
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Journal of Hand Surgery, 1993
A case of Ewing’s sarcoma of the thumb is reported, the literature reviewed and the appropriate treatment for this condition discussed.
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A case of Ewing’s sarcoma of the thumb is reported, the literature reviewed and the appropriate treatment for this condition discussed.
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Skeletal Radiology, 1996
A lytic lesion with soft-tissue extension in the sacrum of a 47-year-old man was needle-biopsied under computed tomographic (CT) guidance using an 18-gauge cutting needle. The cytologic appearance of the lesion and immunohistochemical staining were diagnostic of Ewing's sarcoma.
N D, Baker, D M, Dorfman
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A lytic lesion with soft-tissue extension in the sacrum of a 47-year-old man was needle-biopsied under computed tomographic (CT) guidance using an 18-gauge cutting needle. The cytologic appearance of the lesion and immunohistochemical staining were diagnostic of Ewing's sarcoma.
N D, Baker, D M, Dorfman
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The American Journal of Surgery, 1948
Abstract 1. 1. A case of Ewing sarcoma of the fifth left rib is described. 2. 2. The tumor had reached astonishinglyl great size before the patient was received for treatment. 3. 3. The diagnosis was made by aspiration biopsy and supporting evidence is afforded by the rapid and very marked radiosensitivity displayed by the tumor. 4. 4.
E M, KENT, F S, ASHBURN
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Abstract 1. 1. A case of Ewing sarcoma of the fifth left rib is described. 2. 2. The tumor had reached astonishinglyl great size before the patient was received for treatment. 3. 3. The diagnosis was made by aspiration biopsy and supporting evidence is afforded by the rapid and very marked radiosensitivity displayed by the tumor. 4. 4.
E M, KENT, F S, ASHBURN
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Ewing’s sarcoma of the patella
Skeletal Radiology, 2013Ewing's sarcoma is a relatively rare malignancy, occurring mainly between 4 and 25 years of age. It usually arises from the pelvis, followed by the femur, tibia, and remainder of both the long bones of the extremities and flat bones of the axial skeleton.
Natalia, Gorelik +3 more
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Cancer, 1986
Ewing's sarcoma is a small cell malignant tumor that usually arises in the medullary cavity of bone. Less frequently, it originates in soft tissue and may secondarily invade underlying bone. The origin of Ewing's sarcoma in a periosteal location without extension into either the bone or adjacent soft tissue has not been clearly documented.
S M, Bator +3 more
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Ewing's sarcoma is a small cell malignant tumor that usually arises in the medullary cavity of bone. Less frequently, it originates in soft tissue and may secondarily invade underlying bone. The origin of Ewing's sarcoma in a periosteal location without extension into either the bone or adjacent soft tissue has not been clearly documented.
S M, Bator +3 more
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