用杜匹单抗治疗最初假定的特应性皮炎后出现的多系统朗格汉斯细胞组织细胞增生症:极易混淆的病例报告。

IF 0.9 Q4 DERMATOLOGY Case Reports in Dermatology Pub Date : 2024-07-01 eCollection Date: 2024-01-01 DOI:10.1159/000539704
Wenhao Cheng, Hong Ren, Wenlong Hu
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引用次数: 0

摘要

简介特应性皮炎(AD)是一种常见的慢性、复发性、非感染性炎症性皮肤病。杜比鲁单抗是一种人类单克隆抗体,对严重的特应性皮炎有临床疗效,而且安全性良好:我们在此描述一例以前未报道过的多系统朗格汉斯细胞组织细胞增生症(MS-LCH)病例,该病例与使用杜匹单抗治疗AD的病史有关:本文首次描述了一例MS-LCH病例,患者曾接受过杜比单抗治疗AD。该病例突出表明,鉴于LCH易累及皮肤,因此需要将其作为既有疗法无法改善的皮肤病变的鉴别诊断。
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Multisystem Langerhans Cell Histiocytosis following Treatment of Initially Presumed Atopic Dermatitis with Dupilumab: A Case Report of an Extremely Confusing Scenario.

Introduction: Atopic dermatitis (AD) is a common chronic, recurrent, and non-infectious inflammatory skin disease. Dupilumab is a human monoclonal antibody with clinical efficacy in severe AD and has a good safety profile.

Case presentation: We hereby describe a previously unreported case of multisystem Langerhans cell histiocytosis (MS-LCH) that is associated with a history of AD treatment using dupilumab.

Conclusion: A single case of MS-LCH with a history of dupilumab treatment for AD was described for the first time. This case highlights that given its susceptibility to skin involvement, LCH needs to be considered as a differential diagnosis for skin lesions that are not improved by established therapies.

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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
57
审稿时长
9 weeks
期刊最新文献
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