Bergman R
Department of Dermatology, Rambam Medical Center, Haifa, Israel.
Am J Dermatopathol. 1999 Apr;21(2):185-92. doi: 10.1097/00000372-199904000-00015.
Routine histologic study usually is insufficient to subclassify epidermolysis bullosa (EB); currently, electron microscopic evaluation has been the gold standard. A major advance recently has been made in elucidating the molecular basis of several major forms of EB. Concomitantly, immunoreagents have been developed to map antigens in the basement membrane zone. Some of these reagents facilitate the classification of EB into types and subtypes and can be used as an adjunct informative screening procedure to direct mutation identification efforts using DNA technologies. The current review provides an overview of these recent developments and a more detailed account of the immunohistopathologic diagnosis of EB.
常规组织学研究通常不足以对大疱性表皮松解症(EB)进行亚分类;目前,电子显微镜评估一直是金标准。最近在阐明几种主要形式的EB的分子基础方面取得了重大进展。与此同时,已经开发出免疫试剂来绘制基底膜区的抗原。其中一些试剂有助于将EB分类为不同类型和亚型,并且可以用作辅助性信息筛选程序,以指导使用DNA技术进行的突变鉴定工作。本综述概述了这些最新进展,并更详细地介绍了EB的免疫组织病理学诊断。