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使用度普利尤单抗治疗最初诊断为特应性皮炎后出现的多系统朗格汉斯细胞组织细胞增多症:一个极其复杂病例的报告

Multisystem Langerhans Cell Histiocytosis following Treatment of Initially Presumed Atopic Dermatitis with Dupilumab: A Case Report of an Extremely Confusing Scenario.

作者信息

Cheng Wenhao, Ren Hong, Hu Wenlong

机构信息

Department of Dermatology, The Affiliated Lianyungang Hospital of Xuzhou Medical University, Lianyungang, China.

The First Affiliated Hospital of Kangda College of Nanjing Medical University, Lianyungang, China.

出版信息

Case Rep Dermatol. 2024 Jul 1;16(1):181-185. doi: 10.1159/000539704. eCollection 2024 Jan-Dec.

Abstract

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.

摘要

引言

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。度普利尤单抗是一种人源单克隆抗体,对重度AD具有临床疗效且安全性良好。

病例报告

我们在此描述一例先前未报告的多系统朗格汉斯细胞组织细胞增生症(MS-LCH)病例,该病例与使用度普利尤单抗治疗AD的病史相关。

结论

首次描述了一例有使用度普利尤单抗治疗AD病史的MS-LCH病例。该病例强调,鉴于LCH易累及皮肤,对于经既定治疗后未改善的皮肤病变,需要将LCH作为鉴别诊断考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3482/11250504/fbd0e8c3889e/cde-2024-0016-0001-539704_F01.jpg

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