Suppr超能文献

再探“表皮内上皮瘤”:对博斯特-雅达索恩现象的免疫组织化学研究

The "intraepidermal epithelioma" revisited: immunohistochemical study of the borst-jadassohn phenomenon.

作者信息

Lora Viviana, Chouvet Brigitte, Kanitakis Jean

机构信息

Laboratory of Dermatopathology, Ed. Herriot Hospital, Lyon, France.

出版信息

Am J Dermatopathol. 2011 Jul;33(5):492-7. doi: 10.1097/DAD.0b013e3181fe6f90.

Abstract

The true nature of the so-called intraepidermal epithelioma of Borst-Jadassohn is poorly understood; whether this represents a distinct tumor or a morphological phenomenon [Borst-Jadassohn phenomenon (BJP)] shared by different entities has been debated. So far, no detailed immunohistochemical studies have been performed to address this issue. The aim of our study was to get further insight into the pathogenesis of the intraepidermal epithelioma of Borst-Jadassohn/BJP. Tumors showing the BJP [mainly clonal seborrheic keratoses (cSK) and clonal Bowen disease (cBD)] were studied and compared with typical (nonclonal) counterparts. Cell nests in cSK, cBD, hidroacanthoma simplex (HS), and porocarcinoma (PC) showed strong expression of epidermal growth factor-receptors (EGF-R), Ki-67, p63, and p53. Cell nests of clonal SK and HS (but not of clonal BD or PC) expressed keratin 5/6. The expression of E-cadherin and the number of CD1a+ Langerhans cells were reduced within the nests of all lesions, whereas melanocytes were increased in all of them. Keratins 7 and 19 were not expressed in any of the lesions. Tumors showing the BJP exhibit some immunohistochemical differences, suggesting that they represent separate entities. However, they all show strong expression of EGF-R within intraepidermal keratinocyte nests, suggesting that the epithelial growth factor pathway plays a role in the development of the BJP.

摘要

所谓的博斯特-雅达松表皮内上皮瘤的真实本质目前仍知之甚少;它是一种独特的肿瘤还是不同实体所共有的一种形态学现象[博斯特-雅达松现象(BJP)],一直存在争议。迄今为止,尚未进行详细的免疫组织化学研究来解决这一问题。我们研究的目的是进一步深入了解博斯特-雅达松表皮内上皮瘤/BJP的发病机制。对表现出BJP的肿瘤[主要是克隆性脂溢性角化病(cSK)和克隆性鲍恩病(cBD)]进行了研究,并与典型的(非克隆性)对应肿瘤进行了比较。cSK、cBD、单纯性汗腺棘皮瘤(HS)和汗孔癌(PC)中的细胞巢显示表皮生长因子受体(EGF-R)、Ki-67、p63和p53呈强表达。克隆性SK和HS(但不包括克隆性BD或PC)的细胞巢表达角蛋白5/6。所有病变的细胞巢内E-钙黏蛋白的表达和CD1a+朗格汉斯细胞的数量均减少,而所有病变中的黑素细胞均增多。所有病变均未表达角蛋白7和19。表现出BJP现象的肿瘤存在一些免疫组织化学差异,提示它们代表不同的实体。然而,它们在表皮内角化细胞巢内均显示EGF-R的强表达,提示上皮生长因子途径在BJP的发生发展中起作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验