Steffen Charles
Am J Dermatopathol. 2005 Feb;27(1):68-85. doi: 10.1097/01.dad.0000144160.26647.ab.
In this historical review I will synopsize the original articles by Lloyd W. Ketron and M.H. Goodman who described Ketron-Goodman disease, by Frederic Woringer and Pierre Kolopp who described Woringer-Kolopp disease, and by Otto Braun-Falco and colleagues who described pagetoid reticulosis. In their publications, each of these authors reported on one patient. I will review the clinical picture of the three patients, their histopathology, and the pathogenesis of each disease as suggested by the above authors. Then the views of others that have written on the subject recently will be reviewed particularly as to their conception of the diseases. Publications that describe the histopathology of the patch (early) stage of mycosis fungoides will be redacted to compare it to the histopathology of Ketron-Goodman disease, Woringer-Kolopp disease, and pagetoid reticulosis. I will discuss whether any or all of them are diseases sui generis, whether they are one, two, or three entities, or whether any or all are but forms of mycosis fungoides.
在这篇历史回顾中,我将概述劳埃德·W·凯特朗(Lloyd W. Ketron)和M·H·古德曼(M.H. Goodman)描述凯特朗 - 古德曼病(Ketron - Goodman disease)的原始文章,弗雷德里克·沃林格(Frederic Woringer)和皮埃尔·科洛普(Pierre Kolopp)描述沃林格 - 科洛普病(Woringer - Kolopp disease)的文章,以及奥托·布劳恩 - 法尔科(Otto Braun - Falco)及其同事描述派杰样网状细胞增生症(pagetoid reticulosis)的文章。在他们的出版物中,这些作者每人都报告了一名患者。我将回顾这三名患者的临床表现、组织病理学,以及上述作者所提出的每种疾病的发病机制。然后将特别回顾近期就该主题撰写文章的其他人的观点,尤其是他们对这些疾病的概念。将编辑描述蕈样肉芽肿斑块(早期)阶段组织病理学的出版物,以便将其与凯特朗 - 古德曼病、沃林格 - 科洛普病和派杰样网状细胞增生症的组织病理学进行比较。我将讨论它们中的任何一种或全部是否为独特的疾病,它们是一种、两种还是三种实体,或者它们中的任何一种或全部是否只是蕈样肉芽肿的形式。