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囊性全毛囊瘤的免疫组织化学剖析:聚焦多种毛囊谱系标志物的表达并深入探讨其发病机制

Immunohistochemical dissection of cystic panfolliculoma focusing on the expression of multiple hair follicle lineage markers with an insight into the pathogenesis.

作者信息

Fukuyama Masahiro, Sato Yohei, Yamazaki Yoshimi, Ohyama Manabu

机构信息

Department of Dermatology, Kyorin University School of Medicine, Tokyo, Japan.

出版信息

J Cutan Pathol. 2017 Oct;44(10):861-866. doi: 10.1111/cup.12992. Epub 2017 Jul 24.

Abstract

Panfolliculoma (PF) is a rare benign tumor with signs of differentiation toward all components of the hair follicle (HF). Cystic panfolliculoma (CPF) is a subset of PF with histological similarity to trichofolliculoma making the differential diagnosis difficult in some cases. Immunohistopathological investigations of PF have been reported; however, previous studies focused mostly on the expression profile of the outer root sheath markers. Herein, we report a case of CPF. A panel of antibodies was developed and used for the detection of the expression of cytokeratin (CK) 10, CK13, CK14, CK15, hair-hard keratin (AE13) and EpCAM within the lesion, supporting the differentiation of all epithelial lineages of the HF and the diagnosis of CPF. Immunohistopathological examinations clearly showed the spatial distribution pattern of each subset of tumor cells with distinct HF differentiation marker expression. Intriguingly, fibroblastic dermal cells were distributed preferentially near CK15-negative epithelium or CK13-positive HF-like structures, suggesting a role for epithelial-mesenchymal interactions (EMIs) in CPF pathogenesis. Further characterization of EMIs between the tumor and surrounding mesenchymal cells in CPF may provide an explanation for immature HF differentiation. These findings suggest that the more intense and coordinated EMI in the analogous tumorigenesis gives rise to mature HF structures, resulting in trichofolliculoma, which may explain their histological resemblance.

摘要

全毛囊瘤(PF)是一种罕见的良性肿瘤,具有向毛囊(HF)所有成分分化的迹象。囊性全毛囊瘤(CPF)是PF的一个亚型,其组织学特征与毛发滤泡瘤相似,这使得在某些情况下鉴别诊断较为困难。已有关于PF的免疫组织病理学研究报道;然而,以往的研究大多集中在外根鞘标志物的表达谱上。在此,我们报告一例CPF病例。我们研发了一组抗体,并用于检测病变内细胞角蛋白(CK)10、CK13、CK14、CK15、毛发硬角蛋白(AE13)和上皮细胞黏附分子(EpCAM)的表达,支持HF所有上皮谱系的分化及CPF的诊断。免疫组织病理学检查清楚地显示了具有不同HF分化标志物表达的肿瘤细胞各亚群的空间分布模式。有趣的是,成纤维细胞性真皮细胞优先分布在CK15阴性上皮或CK13阳性HF样结构附近,提示上皮-间质相互作用(EMIs)在CPF发病机制中发挥作用。进一步阐明CPF中肿瘤与周围间充质细胞之间的EMIs可能为未成熟HF分化提供解释。这些发现表明,在类似的肿瘤发生过程中,更强烈且协调的EMIs会产生成熟的HF结构,从而形成毛发滤泡瘤,这可能解释了它们在组织学上的相似性。

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