Ossifying fibromyxoid tumor of soft parts in a child: A case report

Ossifying fibromyxoid tumor (OFMT) is a relatively rare tumor, most of which occur in adults with preferential localization in subcutis or muscles of the extremeties. Although Schwannian or cartilage origin has been suggested, histogenesis of this tumor still is unclear. The authors present a 6-year...

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Veröffentlicht in:Journal of pediatric surgery 1999-08, Vol.34 (8), p.1294-1296
Hauptverfasser: Ijiri, Rieko, Tanaka, Yukichi, Misugi, Kazuaki, Sekido, Kenichi, Nishi, Toshiji
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container_end_page 1296
container_issue 8
container_start_page 1294
container_title Journal of pediatric surgery
container_volume 34
creator Ijiri, Rieko
Tanaka, Yukichi
Misugi, Kazuaki
Sekido, Kenichi
Nishi, Toshiji
description Ossifying fibromyxoid tumor (OFMT) is a relatively rare tumor, most of which occur in adults with preferential localization in subcutis or muscles of the extremeties. Although Schwannian or cartilage origin has been suggested, histogenesis of this tumor still is unclear. The authors present a 6-year-old girl with retroperitoneal OFMT showing paraspinal extension, who is alive and tumor free 9 years after excision. The current case is the youngest reported patient showing unusual deep trunk site with surgically identified association with the spinal nerve. Both the clinical and histopathologic features strongly suggested Schwannian origin of this tumor.
doi_str_mv 10.1016/S0022-3468(99)90175-6
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subjects Abdomen
Biological and medical sciences
Child
Dermatology
Female
Fibroma, Ossifying - pathology
Humans
Medical sciences
Retroperitoneal Neoplasms - pathology
Soft Tissue Neoplasms - pathology
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Surgery of the digestive system
Tumors of the skin and soft tissue. Premalignant lesions
title Ossifying fibromyxoid tumor of soft parts in a child: A case report
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