Results 171 to 180 of about 39,976 (222)
Some of the next articles are maybe not open access.
Journal of Surgical Oncology, 1980
AbstractFibrosarcomas of the colon are extremely rare. This is the report of a patient with fibrosarcoma of the transverse colon who had perforation and peritonitis.
J L, Hoehn, G H, Hamilton, E, Beltaos
exaly +3 more sources
AbstractFibrosarcomas of the colon are extremely rare. This is the report of a patient with fibrosarcoma of the transverse colon who had perforation and peritonitis.
J L, Hoehn, G H, Hamilton, E, Beltaos
exaly +3 more sources
Plastic and Reconstructive Surgery, 1958
Abstract A case of fibrosarcoma of the tongue is reported. This patient underwent wide local excision of the lesion and is alive and well without extension or recurrence six years postoperatively. Fibrosarcoma is a most unusual type of tumor of the tongue and the occasional long-term survival offered by wide local excision is exemplified by this ...
E J, GARVIN, H E, MARX
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Abstract A case of fibrosarcoma of the tongue is reported. This patient underwent wide local excision of the lesion and is alive and well without extension or recurrence six years postoperatively. Fibrosarcoma is a most unusual type of tumor of the tongue and the occasional long-term survival offered by wide local excision is exemplified by this ...
E J, GARVIN, H E, MARX
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Urology, 1980
A case of fibrosarcoma of the kidney is presented. Clinical and radiologic features are discussed. The arteriographic features of this tumor are indistinguishable from adenocarcinoma of the kidney. Microscopically, this tumor may be confused easily with leiomyoma or leiomyosarcoma, Special staining techniques with van Gieson and Mallory trichrome ...
V, Kansara, I, Powell
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A case of fibrosarcoma of the kidney is presented. Clinical and radiologic features are discussed. The arteriographic features of this tumor are indistinguishable from adenocarcinoma of the kidney. Microscopically, this tumor may be confused easily with leiomyoma or leiomyosarcoma, Special staining techniques with van Gieson and Mallory trichrome ...
V, Kansara, I, Powell
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American Journal of Ophthalmology, 1969
A 3-year-old white girl was seen initially at the Jules Stein Eye Institute in October 1967. At that time, she had a two-month his tory of progressive ptosis, then proptosis, of the left eye. Three weeks before examina tion, she had undergone excisional biopsy of two "apparently encapsulated" nodules of the left upper eyelid.
D E, Eifrig, R Y, Foos
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A 3-year-old white girl was seen initially at the Jules Stein Eye Institute in October 1967. At that time, she had a two-month his tory of progressive ptosis, then proptosis, of the left eye. Three weeks before examina tion, she had undergone excisional biopsy of two "apparently encapsulated" nodules of the left upper eyelid.
D E, Eifrig, R Y, Foos
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Skeletal Radiology, 1986
The records of 14 patients with fibrosarcoma of the jaws--10 in the mandible and four in the maxilla--from the files of the Netherlands Committee on Bone Tumours were studied. The mean age of the patients was 30 years; more men than women were involved; pain and especially swelling were the symptoms most frequently present.
W K, Taconis, T G, van Rijssel
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The records of 14 patients with fibrosarcoma of the jaws--10 in the mandible and four in the maxilla--from the files of the Netherlands Committee on Bone Tumours were studied. The mean age of the patients was 30 years; more men than women were involved; pain and especially swelling were the symptoms most frequently present.
W K, Taconis, T G, van Rijssel
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Cancer, 1976
The pathologic features and the behavior of 53 cases of infantile fibrosarcoma are presented. The tumor nearly always occurred during the first 2 years of life; 41 of the 53 cases occurred during the first, six during the second, and three each during the third and fourth year of life, respectively. Twenty of the 53 cases were present at birth.
E B, Chung, F M, Enzinger
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The pathologic features and the behavior of 53 cases of infantile fibrosarcoma are presented. The tumor nearly always occurred during the first 2 years of life; 41 of the 53 cases occurred during the first, six during the second, and three each during the third and fourth year of life, respectively. Twenty of the 53 cases were present at birth.
E B, Chung, F M, Enzinger
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Journal of Pediatric Surgery, 1987
Congenital fibrosarcoma is a rare fibrous tissue malignancy occurring most commonly in the extremities (71%), but presenting in axial locations as well (29%). Two of our five patients had lower extremity tumors and three had axial lesions located in the thoracolumbar region and anterior neck.
S, Blocker, J, Koenig, J, Ternberg
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Congenital fibrosarcoma is a rare fibrous tissue malignancy occurring most commonly in the extremities (71%), but presenting in axial locations as well (29%). Two of our five patients had lower extremity tumors and three had axial lesions located in the thoracolumbar region and anterior neck.
S, Blocker, J, Koenig, J, Ternberg
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Oral Surgery, Oral Medicine, Oral Pathology, 1988
Ameloblastic fibrosarcoma is an extremely rare tumor. To date only 43 cases have been reported in the literature. An additional case of ameloblastic fibrosarcoma is presented; the clinical features, histologic characteristics, treatment, and the relevance of the presence of dental hard tissue are discussed.
R M, Wood +3 more
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Ameloblastic fibrosarcoma is an extremely rare tumor. To date only 43 cases have been reported in the literature. An additional case of ameloblastic fibrosarcoma is presented; the clinical features, histologic characteristics, treatment, and the relevance of the presence of dental hard tissue are discussed.
R M, Wood +3 more
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European Urology, 1980
A case of retroperitoneal fibrosarcoma is reported. Clinical and pathological signs of the lesion and its treatment are emphasized.
D, Remzi, A, Akdas, C, Tasar, S, Ruacan
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A case of retroperitoneal fibrosarcoma is reported. Clinical and pathological signs of the lesion and its treatment are emphasized.
D, Remzi, A, Akdas, C, Tasar, S, Ruacan
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International Journal of Pediatric Otorhinolaryngology, 1993
A case of an ameloblastic fibrosarcoma in the mandible is described. The primary tumor was seen in a 5-year-old child. In spite of repeated surgical interventions, the tumor recurred three times within a one and a half year period, but not metastases have been observed.
B, Sözeri +3 more
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A case of an ameloblastic fibrosarcoma in the mandible is described. The primary tumor was seen in a 5-year-old child. In spite of repeated surgical interventions, the tumor recurred three times within a one and a half year period, but not metastases have been observed.
B, Sözeri +3 more
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