Harvell J D, Kilpatrick S E, White W L
Department of Pathology, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
Am J Dermatopathol. 1998 Aug;20(4):339-45. doi: 10.1097/00000372-199808000-00003.
The authors describe three lesions that provide further evidence for a close, possibly histogenetic relation between giant cell fibroblastoma and dermatofibrosarcoma protuberans. The first case involves a dermatofibrosarcoma protuberans that contained a single giant cell fibroblastoma-like focus of multi-nucleate giant cells. A second tumor, a giant cell fibroblastoma, recurred 6 years later as a dermatofibrosarcoma protuberans. In the third lesion, there was a juxtaposition and co-mingling of dermatofibrosarcoma protuberans and giant cell fibroblastoma within the same primary lesion. In all cases, both the giant cell fibroblastoma areas and dermatofibrosarcoma protuberans areas stained positively with CD34. A fourth case, a dermatofibrosarcoma protuberans infiltrated skeletal muscle, creating giant cell fibroblastoma-like giant cell mimics--a result of skeletal muscle degeneration or atrophy with nuclear conglomeration. The latter giant cells failed to express CD34 but did show immunoreactivity with desmin. These findings support the concept that giant cell fibroblastoma and dermatofibrosarcoma protuberans probably represent a histologic spectrum of a single CD34 positive (perhaps, dermal dendrocytic) neoplasm, a conclusion supported by a recently cloned t(7;22) breakpoint demonstrated in both neoplasms.
作者描述了三个病变,这些病变为巨细胞纤维母细胞瘤与隆突性皮肤纤维肉瘤之间存在密切的、可能是组织发生学上的关系提供了进一步的证据。第一例是一个隆突性皮肤纤维肉瘤,其中含有一个单一的多核巨细胞组成的类似巨细胞纤维母细胞瘤的病灶。第二例肿瘤,一个巨细胞纤维母细胞瘤,6年后复发为隆突性皮肤纤维肉瘤。在第三个病变中,在同一原发性病变内隆突性皮肤纤维肉瘤和巨细胞纤维母细胞瘤并列且相互混合。在所有病例中,巨细胞纤维母细胞瘤区域和隆突性皮肤纤维肉瘤区域的CD34染色均为阳性。第四例是一个隆突性皮肤纤维肉瘤浸润骨骼肌,形成了类似巨细胞纤维母细胞瘤的巨细胞假象——这是骨骼肌变性或萎缩伴核聚集的结果。后者的巨细胞不表达CD34,但对结蛋白显示免疫反应性。这些发现支持了这样一种概念,即巨细胞纤维母细胞瘤和隆突性皮肤纤维肉瘤可能代表单一的CD34阳性(可能是真皮树突状细胞)肿瘤的组织学谱系,这一结论得到了最近在这两种肿瘤中均发现的t(7;22)断点克隆的支持。