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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 in Korean | 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.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Prognosis / Recurrence / Osteochondroma / Retrospective Studies / Follow-Up Studies / Chondrosarcoma / Osteochondromatosis / Disease-Free Survival / Enchondromatosis / Neoplasm Metastasis Type of study: Observational study / Prognostic study Limits: Humans Language: Korean Journal: The Journal of the Korean Bone and Joint Tumor Society Year: 2011 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Prognosis / Recurrence / Osteochondroma / Retrospective Studies / Follow-Up Studies / Chondrosarcoma / Osteochondromatosis / Disease-Free Survival / Enchondromatosis / Neoplasm Metastasis Type of study: Observational study / Prognostic study Limits: Humans Language: Korean Journal: The Journal of the Korean Bone and Joint Tumor Society Year: 2011 Type: Article