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Diagnostic Pitfalls in Newborns and Babies with Blisters and Erosions

机译:患有水疱和糜烂的新生儿和婴儿的诊断陷阱

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Establishing the correct diagnosis in newborns presenting with blisters and erosions is not always a straightforward process. Many different disease entities including acquired (i.e., infectious, immunobullous, traumatic) and inherited disorders have to be taken into consideration. Similarities in clinical appearance, colonization and/or superinfections of preexisting skin lesions, as well as the absence of late changes in the neonate often pose significant diagnostic challenges. In this paper we discuss by giving examples the process of making an accurate diagnosis of blistering skin diseases in the neonatal period on the basis of a diagnostic algorithm. In addition, we provide an overview of the rational use and the limitations of laboratory procedures such as microbial testing, routine light microscopy, immunofluorescence antigen mapping, transmission electron microscopy, and molecular genetic analysis.
机译:在出现水泡和糜烂的新生儿中建立正确的诊断并非总是一个简单的过程。必须考虑许多不同的疾病实体,包括获得性(即传染性,免疫性,创伤性)和遗传性疾病。既有皮肤病变的临床外观,定植和/或超级感染的相似性,以及新生儿后期变化的缺乏通常构成重大的诊断挑战。在本文中,我们将通过诊断算法为例,举例说明在新生儿期对水疱性皮肤病进行准确诊断的过程。此外,我们概述了实验室程序的合理使用和局限性,例如微生物检测,常规光学显微镜,免疫荧光抗原图谱,透射电子显微镜和分子遗传分析。

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