Suppr超能文献

掌跖部蕈样肉芽肿样表现的汗疱疹样湿疹:1 例报告。

Mycosis Fungoides Palmaris et Plantaris Mimicking "Dyshidrotic Eczema": A Case Report.

出版信息

J Drugs Dermatol. 2024 Jul 1;23(7):569-570. doi: 10.36849/JDD.8474.

Abstract

Mycosis fungoides palmaris et plantaris (MFPP) is a rare variant of mycosis fungoides (MF), a type of cutaneous T-cell lymphoma. MFPP primarily affects the palms and soles of the feet and is often misdiagnosed as dyshidrotic eczema due to its similar clinical presentation. This case report presents a middle-aged woman with MFPP whose initial presentation was mistaken for dyshidrotic eczema. Despite treatment with topical corticosteroids, the patient's lesions persisted, prompting further investigations that led to the diagnosis of MFPP. The patient was initiated on betamethasone dipropionate ointment and hydroxyzine for pruritus management, with a pivotal referral to oncology for comprehensive evaluation. This case highlights the importance of considering MFPP in the differential diagnosis of persistent eczematous lesions on the palms and soles, especially when treatment with topical corticosteroids is ineffective. J Drugs Dermatol. 2024;23(7):569-570.     doi:10.36849/JDD.8474.

摘要

掌跖部蕈样霉菌病(MFPP)是蕈样霉菌病(MF)的一种罕见变异,MF 是一种皮肤 T 细胞淋巴瘤。MFPP 主要影响手掌和足底,由于其类似的临床表现,常被误诊为汗疱疹样湿疹。本病例报告介绍了一名中年女性患有 MFPP,其初始表现被误诊为汗疱疹样湿疹。尽管接受了外用皮质类固醇治疗,但患者的病变仍持续存在,进一步的检查促使诊断为 MFPP。患者开始使用倍他米松二丙酸酯软膏和羟嗪进行瘙痒管理,并关键转诊到肿瘤学进行全面评估。本病例强调了在手掌和足底持续性湿疹样病变的鉴别诊断中考虑 MFPP 的重要性,特别是在外用皮质类固醇治疗无效时。J 皮肤病药物杂志。2024;23(7):569-570.。    doi:10.36849/JDD.8474.

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