Doric Mirsad, Radovic Svjetlana, Babic Mirsad, Kuskunovic Suada, Tomic Ivana, Hukic Ajna, Selak Ivan
Institute of Pathology, Sarajevo University School of Medicine.
Med Arh. 2006;60(6):389-90.
Giant cell fibroblastoma (GCF) is a rare type of fibroblastic tumor, first described as a juvenile form of dermatofibrosarcoma. Although recurrences are common after local surgical resection, metastasis is not reported.We report a case of a 4-year-old boy with giant cell fibroblastoma, in which the neoplasm was characterized histologically by a proliferation of spindle-shaped cells intermixed with pseudovascular channels called "angiectold spaces". The spaces were lined by large cells with pleomorphic nuclei intermixed with multinucleated cells. Immunohistochemically, the tumor stained diffusely for vimentin and CD34, but negative for S 100 protein. Since the initial description in 1982, less than 100 cases of GCF have been reported. This patient's presentation is particularly interesting because present the first case reported in Bosnia and Herzegovina.
巨细胞成纤维细胞瘤(GCF)是一种罕见的纤维母细胞性肿瘤,最初被描述为皮肤纤维肉瘤的一种青少年型。尽管局部手术切除后复发很常见,但尚未有转移的报道。我们报告一例4岁男孩患巨细胞成纤维细胞瘤,该肿瘤在组织学上的特征是梭形细胞增生并伴有称为“血管样间隙”的假血管通道。这些间隙内衬有核多形性的大细胞,并夹杂有多核细胞。免疫组化显示,肿瘤弥漫性表达波形蛋白和CD34,但S-100蛋白呈阴性。自1982年首次描述以来,报道的GCF病例不到100例。该患者的病例特别有趣,因为这是波斯尼亚和黑塞哥维那报道的首例病例。