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PERIOSTEAL FIBROSARCOMA
MARTIN BATTS, Jr., M.D.
Arch Surg. 1941;42(3):566-576.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings. |
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Primary malignant tumors of bone constitute approximately 1 per cent of all types of malignant neoplasms.1 Of this 1 per cent, an extremely small proportion is made up of periosteal fibrosarcomas. Kolodny,2 in his review of the material in the Bone Registry of Sarcoma in 1928, found only a few cases. Geschickter and Copeland have stated that, among over 1,700 neoplasms involving bone, only 1.5 per cent were placed in this group. In a series of 200 primary malignant bone tumors seen at the University Hospital since 1925, comprising osteogenic sarcoma, Ewing's sarcoma, multiple myeloma and periosteal fibrosarcoma, 27 were included in the last-named group, a relatively high incidence. In every instance the diagnosis was made on the basis of a combination of clinical, operative, roentgen and histologic observations.
GENERAL CONSIDERATIONS
The age distribution in these 27 cases was, in general, that found in most cases of sarcoma.
. . . [Full Text PDF of this Article]
Author Affiliations
GRAND RAPIDS, MICH.
From the Department of Surgery, University of Michigan, the Orthopedic Service of Dr. Carl E. Badgley.
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