Desmoid Tumorの5例

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  • FIVE CASES OF DESMOID TUMORS

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Desmoid tumor is a rare, noncapsulated, nonmetastasizing, yet locally invasive neoplasm arising from musculoaponerotic tissue. It occurs most commonly as an abdominal wall mass in multi-gravida or as an extra-abdominal tumor in a variety of locations, particularly in the shoulder and pelvic girdle areas.<br> Five patients with desmoid tumor who were treated from 1972 to 1984 in the First Department of Surgery, Gifu University, were reviewed. There were two males and three females ranging in age from 24 to 60 years, with a mean age of 49 years. All the patients presented with a firm or hard growing mass.<br> The tumor developed in the abdominal wall in two patients and in the lateral chest, neck and mediastinum in one each.<br> Three patients were treated with resection and two patients were treated with resection in combination with postoperative radiation. At present, all patients are alive and disease free at a mean follow up of 7 years.

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