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Congenital dermatofibrosarcoma protuberans with fibrosarcomatous and myxoid change

机译:先天性皮纤维肉瘤隆突伴纤维肉瘤和粘液样变

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摘要

This report describes a case of congenital dermatofibrosarcoma protuberans (DFSP) with fibrosarcomatous (FS) and myxoid areas. Immunohistochemical results showed that tumour cells in ordinary DFSP areas were diffusely positive for CD34, whereas in the FS and myxoid areas, few tumour cells were positive for this antigen. Ki-67 positive tumour cell numbers were greater in the FS (11.8%) and myxoid areas (19.8%) relative to ordinary DFSP areas (2.2%). Reverse transcription polymerase chain reaction and sequence analysis showed the presence of an identical COL1A1–PDGFB fusion transcript in ordinary DFSP (plaque-like area), FS, and myxoid areas of DFSP. These results indicate that the three components of DFSP have a common histogenesis. This study documents the first application of gene analysis involving the myxoid area of DFSP.
机译:该报告描述了一例先天性皮纤维肉瘤隆突(DFSP)伴有纤维肉瘤(FS)和粘液样区域。免疫组织化学结果显示,普通DFSP区域的肿瘤细胞CD34呈弥漫阳性,而FS和粘液样区域的肿瘤细胞对该抗原呈阳性。相对于普通DFSP区域(2.2%),FS(11.8%)和粘液区域(19.8%)的Ki-67阳性肿瘤细胞数量更大。逆转录聚合酶链反应和序列分析表明,在普通DFSP(噬斑样区域),FS和DFSP粘液区域中存在相同的COL1A1-PDGFB融合转录本。这些结果表明DFSP的三个组件具有共同的组织发生。这项研究记录了涉及DFSP粘液区域的基因分析的首次应用。

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