Suppr超能文献

蕈样肉芽肿患者中出现类似嗜酸性蜂窝织炎(韦尔斯综合征)的嗜酸性浸润。

Eosinophilic infiltrate resembling eosinophilic cellulitis (Wells syndrome) in a patient with mycosis fungoides.

作者信息

Emge Drew A, Lewis Daniel J, Aung Phyu P, Duvic Madeleine

机构信息

Department of Internal Medicine, Baylor College of Medicine, Houston, Texas.

出版信息

Dermatol Online J. 2018 Jan 15;24(1):13030/qt9kq75581.

Abstract

Mycosis fungoides (MF) is a T-cell, non-Hodgkin lymphoma that primarily involves the skin. Extracutaneous involvement, such as in the parotidgland, is characteristic of end-stage disease. Eosinophilic cellulitis, or Wells syndrome, is a rare inflammatory dermatitis that involves a dermal infiltrate of eosinophils. We report a case of an 80-year-old man with a long-standing diagnosis of stage IIB MF who acutely developed parotid gland involvement and marked hypereosinophilia that most likely represented eosinophilic cellulitis. Activated T cells from his MF were likely a trigger factor for the development of his eosinophilic cellulitis. To our knowledge, this is the first reported case of an MF patient with atypical parotid gland involvement andeosinophilic cellulitis.

摘要

蕈样肉芽肿(MF)是一种主要累及皮肤的T细胞非霍奇金淋巴瘤。皮肤外受累,如累及腮腺,是终末期疾病的特征。嗜酸性蜂窝织炎,即韦尔斯综合征,是一种罕见的炎症性皮肤病,其特征为真皮内有嗜酸性粒细胞浸润。我们报告一例80岁男性患者,长期诊断为IIB期MF,急性出现腮腺受累及明显的嗜酸性粒细胞增多,很可能代表嗜酸性蜂窝织炎。来自其MF的活化T细胞可能是其嗜酸性蜂窝织炎发生的触发因素。据我们所知,这是首例报告的MF患者出现非典型腮腺受累及嗜酸性蜂窝织炎的病例。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验