威尔斯综合征

Wells syndrome.

作者信息

Bansal Manish, Rai Tulika, Pandey Shyam S

机构信息

Department of Dermatology and Venereology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, India.

出版信息

Indian Dermatol Online J. 2012 Sep;3(3):187-9. doi: 10.4103/2229-5178.101815.

DOI:10.4103/2229-5178.101815

PMID:23189251

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3505426/

Abstract

Wells syndrome or eosinophilic cellulitis is characterized clinically by an acute dermatitis resembling cellulitis and histopathologically by dermal eosinophilic infiltration. Various morphological presentations have been described. We report a 32-year-old female with recurrent, erythematous plaques on left forearm of 8 months duration, associated with mild itching that resolved leaving mild hyperpigmentation.

摘要

韦尔斯综合征或嗜酸性粒细胞性蜂窝织炎在临床上的特征是类似蜂窝织炎的急性皮炎，在组织病理学上表现为真皮嗜酸性粒细胞浸润。已经描述了各种形态学表现。我们报告一名32岁女性，左前臂反复出现红斑性斑块，持续8个月，伴有轻度瘙痒，消退后留下轻度色素沉着。