神经内分泌癌中骨骼肌标记物的 "异常 "表达:一个重要的诊断陷阱。

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2024-10-01 Epub Date: 2024-06-04 DOI:10.1007/s00428-024-03838-0
Guillermo Garcia-Porrero, Faye Wood, Sara Faria, Paul J Kelly, W Glenn McCluggage
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引用次数: 0

摘要

本研究调查了神经内分泌癌(NECs)中肌肉标记物的表达情况,包括特异性骨骼肌标记物myogenin和myoD1。研究包括来自不同部位的 23 例神经内分泌癌(14 例小细胞神经内分泌癌和 9 例大细胞神经内分泌癌)。研究人员用 desmin、myogenin 和 myoD1 对这些肿瘤进行了染色。在 14 个病例(61%)中观察到至少一种肌肉标记物的阳性染色。其中8例(35%)、8例(35%)和11例(48%)的去蛋白、肌原蛋白和myoD1分别呈阳性。在大多数病例中,但并非所有病例的阳性染色都是局灶性的,一般涉及
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"Aberrant" expression of skeletal muscle markers in neuroendocrine carcinomas: a significant diagnostic pitfall.

In this study, we investigate the expression of muscle markers, including the specific skeletal muscle markers myogenin and myoD1, in neuroendocrine carcinomas (NECs). The study included 23 NECs from various sites (14 small cell NECs and 9 large cell NECs). These were stained with desmin, myogenin and myoD1. Positive staining with at least one muscle marker was observed in 14 cases (61%). 8 (35%), 8 (35%) and 11 (48%) of the cases were positive with desmin, myogenin and myoD1 respectively. In most, but not all, cases positive staining was focal generally involving < 10% of tumour cells. Expression of muscle markers is not uncommon in NECs. This represents an important diagnostic pitfall of which pathologists should be aware. In reporting this phenomenon, we speculate on the pathogenesis of this "aberrant" expression of muscle markers.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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