Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
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Gene/Protein
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Target Concepts:
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Query: UMLS:C0029463 (
osteosarcoma
)
16,637
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Two complications of Paget's disease are presented : they include an
osteogenic sarcoma
and a giant-cell tumour (GCT) of the lumbar spine with a radiculo-medullary compression syndrome. The rarity of sarcomatous degeneration of the spine affected by Paget's disease is emphasized and also the unusual character of the spinal GCT which develop in the presence of Paget's disease. As in the present case, it is often difficult to confirm the benign or malignant character of a GCT and the principal criteria of this classification are discussed.
Rev Rhum
Mal
Osteoartic 1975 Oct
PMID:[Radiculomedullary compressions by osteosarcoma and by giant cell tumor of the spine occurring in Paget's disease]. 110 64
The authors report 12 cases of Paget's disease with sarcomatous degeneration that were observed among 311 patients with Paget's disease hospitalized in the Montpellier Rheumatology Clinic. They compare their experience with information they were able to extract from the literature in French and English. The frequency of such degeneration in cases of Paget's disease is difficult to determine but did not appear to exceed 1%. Degeneration rarely occurred before the age of 50 years, affected men twice as frequently as women, and occurred particularly in cases of diffuse Paget's disease, mainly in the femur or the humerus; the rachis was rarely affected. Pain was the main symptom, was practically constant, was remarkable because of its permanence and its intensity. Tumefaction was frequently seen. Pathological fractures were seen in almost a third of the patients with sarcomas of the long bones. Radiculo-medullary compression characterized the rare cases with involvement of the vertebral column or the sacrum. Radiography showed rupture of cortical layers with invasion of the soft parts without any periostal reaction. Histological investigation confirmed the diagnosis by demonstrating one of the three types of
osteogenic sarcoma
: osteosarcomas were the most frequent. Less frequently giant-cell sarcomas or reticulosarcomas were found. The affected patients nearly always died, survival at five years being rare. Treatment, amputation or radiotherapy, was disappointing.
Rev Rhum
Mal
Osteoartic 1975 Nov
PMID:[Sarcomas associated with Paget's disease]. 122 55
A parosteal
osteosarcoma
of the right radius has developed in a patient treated for a long time by etretinate (total dose: 73 g). If brachial ossifications have been reported to etretinate in 2 cases, they were benign tumours; so coincidence is possible in our case. Nevertheless, a relation between the tumour and the treatment cannot be excluded and justify the report of this observation.
Rev Rhum
Mal
Osteoartic 1991 Nov 30
PMID:[Parosteal sarcoma of the radius in the course of etretinate therapy]. 178 Jun 62
The anatomo-radiological study was conducted in 6 cases of isolated malignant intra-osseous tumours of the hip: 1
osteogenic sarcoma
of the femoral head, 1 supra-acetabular chondrosarcoma, 3 carcinomatous metastases of the femoral head (2 predominantly lytic and 1 osteosclerotic), 1 supra-acetabular carcinomatous metastasis. This study reveals why, in the early stages of the disease and depending on the experience of the observer, the radiological appearance of these lesions can be easily confused with those of various conditions frequently seen by the rheumatologist. The authors also discuss the interactions of the metastases with the biomechanical conditions of the affected bone.
Rev Rhum
Mal
Osteoartic 1985 May
PMID:[Malignant bone tumors of the hip. Anatomo-radiological correlation]. 385 7
A forty-four-year old man was hospitalized for diagnosis and treatment of a left leg ulcer which did not heal despite good compliance with a three-month medical regimen. Twenty years before he had undergone surgical curettage and radiotherapy (81 gy) for an
osteosarcoma
of the upper third of the left tibia. He was considered completely cured with regular findings. On examination he had a 5 X 7 cm deep ulcer with raised margins and no signs of infection, localized on the radiodermatitis on the medial aspect of his left leg. Arterial examination confirmed the left arteriopathy with absence of distal pulses; the Ankle Brachial Pressure Index was 0.69 and the foot TcPO2 27 mmHg. Arteriography confirmed the localized left lesions with three distal popliteal and proximal arterial occlusions, all other arteries being strictly normal. Arterial and dermatological radiation leg ulcer was retained as the etiological diagnosis. As the ulcer was very painful, extensive and limited walking distance, surgical revascularisation was undertaken because endoluminal revascularization was impossible. A femoroperoneal saphenous bypass was performed with surgical incisions beyond the radiodermatitis area. Two months after a split skin graft, the ulcer was considered healed and the patency of the by-pass confirmed on duplex examination. This is the first case report of a successful distal by-pass performed for radiation arteritis and ulcer healing. Long-term follow up should be reported.
J
Mal
Vasc 2006 Feb
PMID:[Radiation arteritis- and radiodermitis-induced leg ulcer: surgical revascularization]. 1660 28