Ijiri R, Tanaka Y, Misugi K, Sekido K, Nishi T
Department of Pathology, Kanagawa Children's Medical Center, Yokohama, Japan.
J Pediatr Surg. 1999 Aug;34(8):1294-6. doi: 10.1016/s0022-3468(99)90175-6.
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.
骨化性纤维黏液样肿瘤(OFMT)是一种相对罕见的肿瘤,大多数发生于成年人,好发于四肢的皮下或肌肉。尽管有人提出其起源于施万细胞或软骨,但该肿瘤的组织发生仍不清楚。作者报告了一名6岁患腹膜后OFMT并伴有椎旁延伸的女孩,在切除术后9年仍存活且无肿瘤。该病例是报告中最年轻的患者,肿瘤位于躯干深部,手术发现与脊神经有关。临床和组织病理学特征均强烈提示该肿瘤起源于施万细胞。