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The Annals of Thoracic Surgery, Vol 40, 535-541, Copyright © 1985 by The Society of Thoracic Surgeons
MK McAfee, PC Pairolero, EJ Bergstralh, JM Piehler, KK Unni, RA McLeod, PE Bernatz and WS Payne
The cases of 96 patients (55 male and 41 female) with primary
chondrosarcoma of the chest wall were reviewed. Ages ranged from 17 to 78
years (median, 53.5 years). The tumor involved the rib in 78 patients and
the sternum in 18. Seventy-two patients had treatment at the Mayo Clinic,
28 by wide resection, 25 by local excision, and 19 by palliative excision.
There was 1 operative death. Follow-up ranged from 1 to 46 years. Recurrent
chondrosarcoma developed in 37 patients. All had local recurrence, and 14
also had metastases. Within 10 years, recurrence had developed in 50% of
patients who had local excision and in 17% of patients who had wide
resection. Ten-year chondrosarcoma survival (Kaplan-Meier) for patients
treated by wide resection was 96%; by local excision, 65%; and by
palliative excision, 14% (p less than 0.0001). Tumor grade, tumor diameter,
tumor location, and date of operation all had a significant influence on
survival. This report documents the natural history of chest wall
chondrosarcoma and demonstrates that early wide resection is the treatment
of choice.
ARTICLES
Chondrosarcoma of the chest wall: factors affecting survival
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