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Bone Sarcomas Arising in Fibrous Dysplasia
A. G. HUVOS; N. L. HIGINBOTHAM; T. R. MILLER
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From the Department of Pathology and the Bone Service of the Department of Surgery, Memorial Hospital for Cancer and Allied Diseases, New York
1972 by The Journal of Bone and Joint Surgery, Incorporated
The Journal of Bone & Joint Surgery.  1972; 54:1047-1056 
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Abstract

Twelve patients with histologically proved sarcoma arising in fibrous dysplasia of bone (six monostotic, six polyostotic) are described. In five (Group I) the existence of the dysplasia was known years before the sarcoma arose, and in seven (Group II) the discovery of both lesions was concurrent. The average age of patients in Group I

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was fifteen years when compared with thirty-five years in Group II. In only one instance could the history of previous radiotherapy be elicited. The histological examination of the primary bone sarcomas revealed eight osteosarcomas, two chondrosarcomas, and two spindle-cell sarcomas.

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    These activities have been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of the American Academy of Orthopaedic Surgeons and The Journal of Bone and Joint Surgery, Inc. The American Academy of Orthopaedic Surgeons is accredited by the ACCME to provide continuing medical education for physicians.
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