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Sarcomatous degeneration in Paget's bone disease
Authors:P. Seret  M. F. Basle  A. Rebel  J. C. Renier  J. P. Saint-Andre  G. Bertrans  M. Audran
Affiliation:(1) Department of Clinical Rheumatology, CHU, 1 Av. de l'Hôtel Dieu, F-49040 Angers Cedex, France;(2) Laboratory of Histology-Embryology, UER Médecine, Rue Haute de Reculée, 49045 Angers Cedex, France;(3) Laboratory of Pathology, CHU, 1 Av. de l'Hôtel Dieu, F-49040 Angers Cedex, France;(4) Laboratory of Pathology, Centre Anti-Cancéreux Paul Papin, 2, Rue Moll, F-49036 Angers Cedex, France
Abstract:Summary The authors report 12 cases (8 men and 4 women) of sarcomatous degeneration in Paget's bone disease, with an average age of 72.3 years. Sarcomatous degeneration occurred often in polyostotic Paget's disease, and osteitis deformans was seen in 4 cases. Femur and pelvis were the most affected bones. Pain was a constant feature, whereas tumefaction and fracture were less common. Osteolytic lesions were more frequent than condensed or mixed lesions and radiological signs of malignancy were usually found. Seven cases were histologically clasiified as osteogenic sarcoma and 3 cases as fibrosarcoma. Electron microscopy was performed on 2 osteogenic sarcomas and in 1 case revealed microcylindrical inclusion in Pagetic osteoclasts and in multinucleated giant tumor cells, but none in mononucleated tumor cells. The average survival time for the patients in this study was only 4.5 months.
Keywords:Paget's disease of bone  Osteosarcoma  Electron microscopy
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