An update on selected cutaneous (myo) fibroblastic mesenchymal tumors

IF 2.9 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Natalia Georgantzoglou , Konstantinos Linos
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引用次数: 0

Abstract

Cutaneous (myo)fibroblastic tumors constitute a group of tumors with overlapping clinicopathological features and variable biologic behavior. In the present review we focus on the histomorphology, immunohistochemical profile and molecular background of the following entities: dermatofibrosarcoma protuberans (DFSP), CD34-positive fibroblastic tumor (SCD34FT), myxoinflammatory sarcoma (MIFS), low-grade myofibroblastic sarcoma, solitary fibrous tumor and nodular fasciitis. Although some of these entities typically arise in deep-seated locations, they may occasionally present as cutaneous/superficial tumors and might be challenging to recognize. This review covers in depth the latest advances in molecular diagnostics and immunohistochemical markers that have significantly facilitated the correct classification and diagnosis of these neoplasms.

选定的皮肤(肌)成纤维细胞间充质肿瘤的最新进展
皮肤(肌)成纤维细胞肿瘤是一组临床病理特征重叠、生物学行为多变的肿瘤。在本综述中,我们重点介绍了以下实体的组织形态学、免疫组织化学特征和分子背景:隆起性皮肤纤维肉瘤(DFSP)、CD34阳性成纤维细胞瘤(SCD34FT)、黏液炎性肉瘤(MIFS)、低度肌成纤维细胞肉瘤、孤立性纤维瘤和结节性筋膜炎。尽管其中一些实体通常出现在深层位置,但它们偶尔可能表现为皮肤/浅表肿瘤,可能难以识别。这篇综述深入报道了分子诊断和免疫组织化学标记物的最新进展,这些进展显著促进了这些肿瘤的正确分类和诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.80
自引率
0.00%
发文量
69
审稿时长
71 days
期刊介绍: Each issue of Seminars in Diagnostic Pathology offers current, authoritative reviews of topics in diagnostic anatomic pathology. The Seminars is of interest to pathologists, clinical investigators and physicians in practice.
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