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Desmoplastic Fibroma Report of Tex Cases and Review of the Literature
WALTER N. RABHAN; JUAN ROSAI
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Department of Surgery, Division of Orthopedic Surgery, and the Department of Pathology, Division of Surgical Pathology, Washington University School of Medicine, and Barnes Hospital, St. Louis
1968 by The Journal of Bone and Joint Surgery, Incorporated
The Journal of Bone & Joint Surgery.  1968; 50:487-502 
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Abstract

Ten cases of desmoplastic fibroma are reported, and fifteen cases from the literature are reviewed. Men and women are equally affected, with the majority of these tumors occurring in the second decade of the patient's life. The diagnosis is made on the histological appearance, which classically shows small elongated fibroblasts surrounded by thick bundles of collagen fibers. There was local recrudescense in three of the ten cases. In no instance were metastases encountered. The treatment of choice is adequate wide local excision. There appeared to be a correlation between the cellularity of the lesion and the incidence of recurrence. Desmoplastic fibroma is a benign lesion, which in some ways parallels proliferative fibromatosis and softtissue desmoid tumors.

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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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