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RETICULUM-CELL SARCOMA OF BONE
John C. Ivins; David C. Dahlin
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Section of Orthopaedic Surgery, Mayo Clinic Division of Surgical Pathology, Mayo Clinic
1953 by The American Orthopaedic Association, Inc.
The Journal of Bone & Joint Surgery.  1953; 35:835-866 
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Abstract

In a survey of 2,000 specimens of primary tumor of bone, forty-nine were found to be reticulum-cell sarcomata. The survey reinforced our conception that reticulum-cell sarcoma is a firmly established entity. It is important to establish the diagnosis by adequate biopsy. Unlike most other primary malignant conditions of bone, reticulum-cell sarcoma appears to be radiosensitive and, in one case in which the tumor disappeared, administration of Coley's toxins was the only treatment. At present, it appears that the prognosis in cases of reticulum-cell sarcoma of bone is significantly better than that in most other primary malignant tumors of bone.

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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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