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首页> 外文期刊>Journal of cutaneous pathology >Pleomorphic fibroma of the skin with MDM2 immunoreactivity: A potential diagnostic pitfall
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Pleomorphic fibroma of the skin with MDM2 immunoreactivity: A potential diagnostic pitfall

机译:具有MDM2免疫反应性的皮肤的亲属纤维瘤:潜在的诊断陷阱

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摘要

Pleomorphic fibroma is a rare benign cutaneous neoplasm characterized by spindle‐shaped cells and multinucleated giant cells scattered throughout collagenous stroma. These morphologic features can lead to diagnostic confusion, including atypical lipomatous tumor as one consideration. In contrast to atypical lipomatous tumor, previous studies have found pleomorphic fibroma to be negative for MDM2 immunohistochemical staining and MDM2 gene amplification. Here, we present a case of pleomorphic fibroma of skin with nuclear MDM2 immunoreactivity in the absence of MDM2 gene amplification, underscoring the superiority of fluorescence in situ hybridization as a diagnostic test in this differential diagnosis. The RB1 locus is also explored for differential diagnosis with pleomorphic/spindle cell lipoma and related entities.
机译:材料纤维瘤是一种稀有的良性皮肤肿瘤,其特征在于纺锤形细胞和散射贯穿胶原基质的多核巨细胞。 这些形态学特征可导致诊断混淆,包括非典型脂质瘤作为一次考虑因素。 与非典型脂质肿瘤形成鲜明对比,先前的研究发现,对于MDM2免疫组织化学染色和MDM2基因扩增,已经发现了最新的纤维瘤。 在这里,我们在没有MDM2基因扩增的情况下呈现具有核MDM2免疫反应性的皮肤纤维纤维瘤的情况,强调了原位杂交的优越性作为这种鉴别诊断中的诊断测试。 还探讨了RB1基因座,用于鉴别诊断,具有含有亲主/主轴细胞脂肪瘤和相关实体的鉴别诊断。

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