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角化不良作为单纯性大疱性表皮松解症-道林·米拉的组织学特征。

Dyskeratosis as a histologic feature in epidermolysis bullosa simplex-Dowling Meara.

作者信息

Bergman Reuven, Harel Avikam, Sprecher Eli

机构信息

Department of Dermatology, Rambam Medical Center and the Bruce Rappaport Faculty of Medicine, Technion-Israel, Institute of Technology, Haifa 31096, Israel.

出版信息

J Am Acad Dermatol. 2007 Sep;57(3):463-6. doi: 10.1016/j.jaad.2007.02.023.

Abstract

BACKGROUND

Intracellular keratin aggregation and clumping is a characteristic ultrastructural feature in epidermolysis bullosa simplex (EBS)-Dowling Meara (DM) yet without histologic correlates in routinely stained specimens.

OBJECTIVE

We sought to detect histologic clues to keratin aggregation and clumping in the involved epidermis of EBS-DM.

METHODS

Four cases of EBS-DM caused by dominant keratin (KRT)5 and KRT14 mutations were studied histologically and ultrastructurally. The histologic slides of 11 additional EBS cases (9 Weber-Cockayne subtypes and two Koebner subtypes) were also reviewed histologically.

RESULTS

Intracytoplasmic aggregation and clumping of tonofilaments were observed ultrastructurally in all 4 EBS-DM cases. Intracytoplasmic eosinophilic homogenizations and inclusions (ie, dyskeratosis) in individual keratinocytes were detected histologically in 3 of the 4 EBS-DM cases, but in none of the 9 EBS-Weber-Cockayne cases or the two EBS-Koebner cases.

LIMITATIONS

This was a relatively small studied group.

CONCLUSION

The histopathological detection of dyskeratosis in individual keratinocytes may provide a valuable clue to keratin aggregation and clumping, and to the diagnosis in EBS-DM.

摘要

背景

细胞内角蛋白聚集和结块是单纯性大疱性表皮松解症(EBS)-Dowling Meara型(DM)的特征性超微结构特征,但在常规染色标本中没有组织学相关性。

目的

我们试图在EBS-DM受累表皮中检测角蛋白聚集和结块的组织学线索。

方法

对4例由显性角蛋白(KRT)5和KRT14突变引起的EBS-DM病例进行组织学和超微结构研究。还对另外11例EBS病例(9例Weber-Cockayne亚型和2例Koebner亚型)的组织学切片进行了组织学检查。

结果

在所有4例EBS-DM病例中,超微结构观察到张力丝的胞浆内聚集和结块。在4例EBS-DM病例中的3例中,组织学检测到单个角质形成细胞内的胞浆嗜酸性均质化和包涵体(即角化不良),但在9例EBS-Weber-Cockayne病例或2例EBS-Koebner病例中均未检测到。

局限性

这是一个相对较小的研究组。

结论

单个角质形成细胞角化不良的组织病理学检测可能为角蛋白聚集和结块以及EBS-DM的诊断提供有价值的线索。

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