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Chondrosarcoma Arising from Benign Bone Tumor due to Malignant Transformation / 대한골관절종양학회지
The Journal of the Korean Bone and Joint Tumor Society ; : 17-22, 2011.
Article Dans Coréen | WPRIM | ID: wpr-172341
ABSTRACT

PURPOSE:

We analyzed the oncological outcome and prognostic factor of the chondrosarcoma arising from benign bone tumor due to malignant transformation. MATERIALS AND

METHODS:

From April 1986 to April 2009, 18 cases were considered eligible. We analyzed retrospectively the patient's characteristics and prognostic factors that affect to the local recurrence and distant metastasis.

RESULTS:

As classified by primary benign bone tumor, 4 cases were solitary osteochondroma, 11 cases were multiple osteochondromatosis and 3 cases were multiple enchondromatosis. The mean follow-up period was 85 months. The 5-year disease free survival rate of 18 patients was 85.9%. Their overall MSTS score was 25.2 (84%). There were local recurrence in 3 cases and no distant metastasis. We found that tumor location and surgical margin affected to the prognosis significantly.

CONCLUSION:

In secondary chondrosarcoma patients, the prognosis was good relatively and tumor location and surgical margin are important prognosis factor.
Sujets)

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Pronostic / Récidive / Ostéochondrome / Études rétrospectives / Études de suivi / Chondrosarcome / Ostéochondromatose / Survie sans rechute / Enchondromatose / Métastase tumorale Type d'étude: Étude observationnelle / Étude pronostique Limites du sujet: Humains langue: Coréen Texte intégral: The Journal of the Korean Bone and Joint Tumor Society Année: 2011 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Pronostic / Récidive / Ostéochondrome / Études rétrospectives / Études de suivi / Chondrosarcome / Ostéochondromatose / Survie sans rechute / Enchondromatose / Métastase tumorale Type d'étude: Étude observationnelle / Étude pronostique Limites du sujet: Humains langue: Coréen Texte intégral: The Journal of the Korean Bone and Joint Tumor Society Année: 2011 Type: Article