Results 211 to 220 of about 30,224 (246)
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Giant cell tumour of bone in a cat
Journal of Small Animal Practice, 1995ABSTRACTA domestic shorthaired cat had a firm, non‐painful swelling of the left antebrachium. Radiographs showed an expansile, multiloculated lesion in the radius. The mass gradually enlarged over the following four and a half months and the animal became completely lame. The histological diagnosis was giant cell tumour of bone; this is a rare neoplasm
B A, Walsh, W H, Rhodes
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Macrophages in giant cell tumours of bone
The Journal of Pathology, 1978Five giant cell tumours of bone were studied to determine the degree of macrophage infiltration and whether the giant cells expressed the characteristics commonly associated with macrophages, i.e., IgGFc and C3 receptors, phagocytosis and non-specific esterase activity.
G W, Wood +3 more
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Angiography in Giant-Cell Tumours of Bone
Acta Radiologica. Diagnosis, 1977The angiographic appearance of 9 cases of genuine giant-cell tumour of bone, 6 cases of aneurysmal bone cyst and one case of non-ossifying fibroma is described. Differential diagnosis would appear to be possible to a certain extent. The non-ossifying fibroma was poorly vascularized.
B, Lundström +3 more
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International Orthopaedics, 1978
The radiological findings in 138 giant-cell tumours in 135 patients, with adequate clinical, radiological, and histological details, were studied. The purpose was to define the characteristic radiographic appearance of giant-cell tumour on presentation and after treatment and to assess whether radiological grading of the tumours was of value in ...
S. M. Tuli +2 more
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The radiological findings in 138 giant-cell tumours in 135 patients, with adequate clinical, radiological, and histological details, were studied. The purpose was to define the characteristic radiographic appearance of giant-cell tumour on presentation and after treatment and to assess whether radiological grading of the tumours was of value in ...
S. M. Tuli +2 more
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The British Journal of Radiology, 1959
The cases referred to in this paper are derived from the Bristol Bone Tumour Registry, and they are gathered from a number of separate orthopaedic and radiotherapeutic centres. For this reason the methods of treatment used have differed from case to case so that we have no considerable number treated by any constant method and cannot produce anything ...
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The cases referred to in this paper are derived from the Bristol Bone Tumour Registry, and they are gathered from a number of separate orthopaedic and radiotherapeutic centres. For this reason the methods of treatment used have differed from case to case so that we have no considerable number treated by any constant method and cannot produce anything ...
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The Journal of Bone and Joint Surgery. British volume, 2004
Giant cell tumour (GCT) is still one of the most obscure and intensively examined tumours of bone. Its histogenesis is uncertain. The histology does not predict the clinical outcome; and there are still many unanswered questions with regard to both its treatment and prognosis.
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Giant cell tumour (GCT) is still one of the most obscure and intensively examined tumours of bone. Its histogenesis is uncertain. The histology does not predict the clinical outcome; and there are still many unanswered questions with regard to both its treatment and prognosis.
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Giant cell tumour of bone in the denosumab era
European Journal of Cancer, 2017Giant cell tumour of bone (GCTB) is an intermediate locally aggressive primary bone tumour, occurring mostly at the meta-epiphysis of long bones. Overexpression of receptor activator of nuclear factor kappa-B ligand (RANKL) by mononuclear neoplastic stromal cells promotes recruitment of numerous reactive multinucleated osteoclast-like giant cells ...
Lizz van der Heijden +2 more
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Telomere biology in giant cell tumour of bone
Journal of Pathology, 2008AbstractGiant cell tumour of bone (GCTB) is a benign bone tumour known for the unpredictable clinical behaviour of recurrences and, in rare instances, distant metastases. It consists of uniformly distributed osteoclastic giant cells in a background of mononuclear rounded and spindle‐shaped cells.
Ramses G Forsyth +2 more
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Radiosensitive giant cell tumour of the sphenoid bone
British Journal of Neurosurgery, 2001Giant cell tumours rarely occur in the cranial region. We encountered a radiosensitive giant cell tumour of the sphenoid in a 12-year-old girl. After a two-stage operation, the residual tumour regrew rapidly. The adjuvant radiotherapy subsequent to additional surgery has suppressed the growth of the residual tumour for 5 years.
Haruhiko Kishima
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International Orthopaedics, 1993
Thirty-one patients with giant cell tumours of bone (BGCT) were treated at our hospital by a conservative approach between 1975 and 1988. 94% of the tumours were grade III (Campanacci) and the follow up was from 2 to 13 years. In the 20 patients who had a modified intralesional excision (curettage) with bone grafting and cement, 5 recurrences occurred.
R J, Rooney +4 more
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Thirty-one patients with giant cell tumours of bone (BGCT) were treated at our hospital by a conservative approach between 1975 and 1988. 94% of the tumours were grade III (Campanacci) and the follow up was from 2 to 13 years. In the 20 patients who had a modified intralesional excision (curettage) with bone grafting and cement, 5 recurrences occurred.
R J, Rooney +4 more
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