Inoue A, Hasegawa T, Ikata T, Hizawa K
Department of Orthopedic Surgery, The University of Tokushima, School of Medicine, Japan.
Clin Orthop Relat Res. 1996 Dec(333):239-44.
A rare case of well differentiated fibrosarcoma occurring in the left second toe is described in a 12-year-old boy who presented with a destructive lesion that had almost totally destroyed the distal phalanx, except for the epiphysis. Amputated specimens showed microscopic evidence of proliferation of uniform spindle cells arranged in both fascicles and a characteristic herringbone pattern with a small number of mitotic figures. This tumor did not show any specific immunoreactivity except for vimentin and had basic ultrastructural characteristics of fibroblasts and myofibroblasts. The tumor was treated by amputation at the middle phalanx level and had not recurred 3 years later. From the presenting radiographic features, some benign neoplasms and reactive lesions were considered in the differential diagnosis. Only results from the pathologic examination were useful in reaching a correct diagnosis.
一名12岁男孩左第二趾发生高分化纤维肉瘤,病例罕见。患儿表现为破坏性病变,除骨骺外,几乎完全破坏了远节指骨。截肢标本显微镜下可见均匀的梭形细胞增殖,呈束状排列,并具有特征性的人字形结构,有少量有丝分裂象。除波形蛋白外,该肿瘤未显示任何特异性免疫反应,具有成纤维细胞和肌成纤维细胞的基本超微结构特征。肿瘤在中节指骨水平行截肢治疗,3年后未复发。根据最初的影像学特征,鉴别诊断考虑了一些良性肿瘤和反应性病变。只有病理检查结果有助于做出正确诊断。