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Ollier's disease is a rare affliction (not more than approximately 100 cases have been reported over a 30-year period) characterized by bone dysplasia in which evolution to degenerative neoplasia has been described. Diagnosis of chondrosarcoma is delicate in these cases. It is a kind of slowly evolving low grade malignant tumor. Surgery is the primary treatment course, and can lead to remission. Prognosis, depending on the number and dimension of the lesions, their localization and metastasis prevention, is usually good, but relapses are relatively frequent: 25 to 50%. In case of relapse, radiotherapy and chemotherapy were tested but their efficacy is limited. We report here two clinical cases and discuss literature data.

Résumé

La maladie d'Ollier est une affection rare caractérisée par une dysplasie osseuse d'origine constitutionnelle dont l'évolution vers la dégénérescence néoplasique est connue. Les cas rapportés ne dépassent pas la centaine en 30 ans. Le diagnostic de chondrosarcome dans ces cas est délicat. Il s'agit d'une tumeur de bas grade de malignité à évolution lente, dont le traitement relève avant tout de la chirurgie, seule capable d'assurer la rémission. En cas de rechute, radiothérapie et chimiothérapie ont été testées mais leur efficacité s'est avérée très réduite. Le pronostic, qui dépend du siège de la lésion, de sa taille, du nombre de foyers et du contrôle local, est relativement favorable mais une récidive survient dans 25 à 50 % des cas. Nous rapportons deux cas cliniques et discuterons des données de la littérature.
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doi:10.1016/j.crad.2005.05.019
Copyright © 2005 The Royal College of Radiologists Published by Elsevier Ltd.

Case Report

A case of multiple chondrosarcomas secondary to severe multiple symmetrical enchondromatosis (Ollier's disease) at an early age
Y. Büktea, , , S. Necmioglub, H. Nazaroglua, N. Kilincc and F. Yilmazc
aDepartment of Radiology, Faculty of Medicine, Dicle University, Diyarbakir, TurkeybDepartment of Orthopaedics, Faculty of Medicine, Dicle University, Diyarbakir, TurkeycDepartment of Pathology, Faculty of Medicine, Dicle University, Diyarbakir, Turkey  相似文献   

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Étude épidémiologique de la scoliose chez les enfants roumains scolarisés     
C. Serbescu  D. Ianc  O. Straciuc  G. Carp  D. Courteix 《Science & Sports》2007,22(6):307-308
The long-term clinical history of this patient from 4 to 22 years highlights the links between severe cerebral palsy and progressive and fixed vertebral deformations.The risk factors in this patient were asymmetrical motor disease and a weakness of righting reactions observed in non ambulatory subjects.Hip dysplasia and painful stiffness of both knees required surgical palliation at the age of 11 and 13 years.Progressive spinal deformation affected both lateral curvatures. The first occurred early, producing a left dorsal curvature with a short radius, the second compensatory curvature affected the the dorsal and lumbar vertebrae producing a right sided curvature with a large radius related to pelvic imbalance.The graphic presentation of the spinal curvatures revealed rapid worsening at puberty.Arthrodesis from D2 to the sacrum was performed at 14.10 years.Given the stiffness of the trunk, it can be expected that the independence of this young adult who lives alone in a flat seated in an electrical wheelchair with assistance for special needs and works half time in the community, may be compromised in the future.
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View Record in Scopus
doi:10.1016/j.scispo.2007.09.009    
Copyright © 2007 Elsevier Masson SAS All rights reserved.

Communication brève

Étude épidémiologique de la scoliose chez les enfants roumains scolarisés
Epidemiological study of scoliosis of Romanian school children  相似文献   

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