Results 211 to 220 of about 61,604 (250)
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Clinical Orthopaedics and Related Research, 1996
Giant cell tumor is a locally aggressive tumor with a high recurrence rate if not completely excised. The condition is more common among Asians than whites. During a 10-year period 44 patients, ranging in age from 12 to 51 years, were treated. The most common sites were the proximal femur and the distal radius.
K M, Yip, P C, Leung, S M, Kumta
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Giant cell tumor is a locally aggressive tumor with a high recurrence rate if not completely excised. The condition is more common among Asians than whites. During a 10-year period 44 patients, ranging in age from 12 to 51 years, were treated. The most common sites were the proximal femur and the distal radius.
K M, Yip, P C, Leung, S M, Kumta
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The Journal of Bone & Joint Surgery, 1952
True giant-cell tumors are quite rare. Solitary bone cysts occur with about the same frequency, while sarcomata of bone are found five times as often as either. We agree with Geschickter and Copeland that. there is a close clinical kinship between giant-cell tumor and solitary bone cyst., and tlsat they probably have a common origin.
M J, STEWART, T R, RICHARDSON
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True giant-cell tumors are quite rare. Solitary bone cysts occur with about the same frequency, while sarcomata of bone are found five times as often as either. We agree with Geschickter and Copeland that. there is a close clinical kinship between giant-cell tumor and solitary bone cyst., and tlsat they probably have a common origin.
M J, STEWART, T R, RICHARDSON
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Clinical Orthopaedics and Related Research, 1986
Giant cell tumor GCT of bone remains a difficult and challenging management problem because there are no absolute clinical, radiographic, or histologic parameters that accurately predict the tendency of any single lesion to recur or metastasize. Enneking's and Campanacci's radiographic classifications and surgical staging are helpful in planning the ...
J J, Eckardt, T J, Grogan
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Giant cell tumor GCT of bone remains a difficult and challenging management problem because there are no absolute clinical, radiographic, or histologic parameters that accurately predict the tendency of any single lesion to recur or metastasize. Enneking's and Campanacci's radiographic classifications and surgical staging are helpful in planning the ...
J J, Eckardt, T J, Grogan
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Radiology, 1947
During the period from Jan. 1, 1942, to Oct. 1, 1945, 656 patients were admitted to an army hospital designated as a radiation therapy center. Of this number, 25 had primary bone tumors, including 10 giant-cell tumors in the diagnosis or treatment of which we participated.
F B, BOGART, A E, IMLER
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During the period from Jan. 1, 1942, to Oct. 1, 1945, 656 patients were admitted to an army hospital designated as a radiation therapy center. Of this number, 25 had primary bone tumors, including 10 giant-cell tumors in the diagnosis or treatment of which we participated.
F B, BOGART, A E, IMLER
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Angiography in Giant-Cell Bone Tumors
Radiology, 1979Angiography was performed on 48 patients with giant-cell bone tumors. Sixty-four per cent were hypervascular; 25% were hypo- or moderately vascular; and 10% were avascular. Findings were similar in the 45 benign and 3 malignant tumors. There was no correlation between the findings and degree of histological aggressiveness.
A, Prando +3 more
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Giant cell tumors of the bones of the hand
The Journal of Hand Surgery, 1997The cases of all patients with a diagnosis of giant cell tumor of bone occurring in the hand and seen at the Mayo Clinic during a 50-year period were reviewed to assess the results of treatment. There were 5 lesions in the phalanges, 7 in the metacarpals, and 1 in the scaphoid.
E A, Athanasian, L E, Wold, P C, Amadio
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Surgical Pathology Clinics, 2012
This article provides an overview of giant cell tumor, including the typical clinical, radiographic, and pathologic findings, as well as some unusual features, such as multifocality and metastases. The article addresses recent advances in the molecular biology of giant cell tumor, particularly receptor activator of nuclear factor kappa B (RANK)-ligand ...
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This article provides an overview of giant cell tumor, including the typical clinical, radiographic, and pathologic findings, as well as some unusual features, such as multifocality and metastases. The article addresses recent advances in the molecular biology of giant cell tumor, particularly receptor activator of nuclear factor kappa B (RANK)-ligand ...
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Multicentric giant-cell tumor of bone
The Journal of Bone & Joint Surgery, 1977The presence of more than one distinct giant-cell tumor in the same patient is rare; seven cases have been reported in the literature. The present series involves eleven patients with thirty-five individual tumors. Multifocal giant-cell tumors may pose a diagnostic problem.
F H, Sim, D C, Dahlin, J W, Beabout
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Giant Cell Tumors of the Sphenoid Bone
Neurosurgery, 1992Giant cell tumors of the sphenoid are rare; there are 36 previously reported cases. We report two cases of these tumors in women in their thirties, both associated with pregnancy. In the first patient, the tumor was removed via a transnasal transsphenoidal approach. In the second patient, a Le Fort maxillotomy was required.
L D, Watkins +4 more
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Giant Cell–Containing Tumors of Bone
Surgical Pathology Clinics, 2017Giant cell-containing tumors of bone are characterized morphologically by the presence of numerous osteoclastic giant cells. Correlation of clinical, radiologic, and laboratory findings is required for accurate histopathologic diagnosis and treatment of a giant cell-containing tumor of bone.
Zsolt Orosz, Nicholas A. Athanasou
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