Results 211 to 220 of about 82,773 (230)
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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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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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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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International Orthopaedics, 1990
Two hundred and thirty-nine patients with Ewing's sarcoma were treated at our institution between 1972 and 1987: 42 of these had lesions in the pelvis, 29 were in the wing of the ilium or involved the sacroiliac joint (type I), 5 were periacetabular (type II), and 8 were in the anterior pelvic arch (type III).
CAPANNA, RODOLFO +5 more
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Two hundred and thirty-nine patients with Ewing's sarcoma were treated at our institution between 1972 and 1987: 42 of these had lesions in the pelvis, 29 were in the wing of the ilium or involved the sacroiliac joint (type I), 5 were periacetabular (type II), and 8 were in the anterior pelvic arch (type III).
CAPANNA, RODOLFO +5 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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Ewing's sarcoma of the retropharynx
The Journal of Laryngology & Otology, 1994AbstractEwing's sarcoma arising in the head and neck region is very rare. A case arising from C2 in a young child is presented. The unusual presentation, differential diagnosis and pathological features are discussed.
J E, O'Connell +3 more
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Ewing's sarcoma of the mandible
Journal of Dentistry, 1976Abstract A case of Ewing's sarcoma in a young girl with the primary in the mandible is presented. Though trauma has not been established as a definite aetiology, it could have been the initiating factor in this case. The patient was treated by surgical excision followed by radiotherapy.
S S, Sidhu, H, Parkash, G L, Subherwal
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Cancer Letters, 2007
Sarcomas account for less than 10% of all human malignancies that are believed to originate from as yet poorly defined mesenchymal progenitor cells. They constitute some of the most aggressive adult and childhood cancers in that they have a high metastatic proclivity and are typically refractory to conventional chemo- and radiation therapy.
Riggi N, Stamenkovic I
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Sarcomas account for less than 10% of all human malignancies that are believed to originate from as yet poorly defined mesenchymal progenitor cells. They constitute some of the most aggressive adult and childhood cancers in that they have a high metastatic proclivity and are typically refractory to conventional chemo- and radiation therapy.
Riggi N, Stamenkovic I
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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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