Suppr超能文献

1例提示演变序列的Dowling-Degos病。

A case of Dowling-Degos disease suggesting an evolutional sequence.

作者信息

Lee S J, Lee H J, Kim D W, Jun J B, Chung S L, Bae H I

机构信息

Department of Dermatology, Kyungpook National University School of Medicine, Taegu, Korea.

出版信息

J Dermatol. 2000 Sep;27(9):591-7. doi: 10.1111/j.1346-8138.2000.tb02234.x.

Abstract

We report a 47-year-old woman who presented with asymptomatic reticulate hyperpigmentations on the neck, lateral face, axillae, trunk, inguinal areas, and dorsa of both hands and feet. We thought it was an unusual case in the spectrum between the pole of Dowling-Degos disease (DDD) and that of reticulate acropigmentation of Kitamura (RAK). Another interesting point was that the biopsied specimens from the abdomen, neck, and axillary lesions showed somewhat different histopathologic features from typical DDD, suggesting an evolutional sequence. From these findings we suggest that a lichenoid inflammation may be responsible for the typical maculo-papular lesions of DDD.

摘要

我们报告了一名47岁女性,其颈部、面部外侧、腋窝、躯干、腹股沟区以及双手和双足背部出现无症状的网状色素沉着。我们认为这是一例处于Dowling-Degos病(DDD)极点与北村网状肢端色素沉着(RAK)极点之间谱系中的不寻常病例。另一个有趣的点是,取自腹部、颈部和腋窝病变的活检标本显示出与典型DDD略有不同的组织病理学特征,提示存在一种演变过程。基于这些发现,我们认为苔藓样炎症可能是DDD典型斑丘疹病变的病因。

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