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一例因度普利尤单抗治疗特应性皮炎诱发银屑病继发乌帕替尼相关性肠梗阻的病例。

A Case of Upadacitinib-Associated Ileus Secondary to Psoriasis Induced by Treatment of Atopic Dermatitis with Dupilumab.

作者信息

Liu Xiaoyang, Mu Zhanglei, Cai Lin

机构信息

Department of Dermatology, Peking University People's Hospital, Beijing, 100044, People's Republic of China.

出版信息

Clin Cosmet Investig Dermatol. 2024 Dec 12;17:2855-2858. doi: 10.2147/CCID.S488354. eCollection 2024.

Abstract

A 69-year-old man with severe atopic dermatitis (AD) received a single 600 mg subcutaneous injection of dupilumab, which resulted in a psoriatic rash on day 10. He was then given 30 mg of oral upadacitinib daily, and after 10 weeks of treatment, both the AD and the psoriasis had significantly improved. However, at week 16, the patient had no bowel movement for a week, and paralytic ileus was suspected based on the patient's symptoms and laboratory findings. Without surgery or other treatment, one week after stopping upadacitinib, the patient resumed bowel movements and the ileus improved, suggesting a possible link between the drug and the ileus, which was considered to be possibly due to the off-target effect of Janus kinase inhibitor (JAKi). This case illustrates the complexity of the immunomodulatory effects of targeted therapies and the need for long-term observation of their mechanisms of action and side effects.

摘要

一名69岁的重度特应性皮炎(AD)患者接受了一次600mg度普利尤单抗皮下注射,在第10天时出现了银屑病皮疹。随后他每天口服30mg乌帕替尼,治疗10周后,AD和银屑病均有显著改善。然而,在第16周时,患者一周没有排便,根据患者症状和实验室检查结果怀疑为麻痹性肠梗阻。在未进行手术或其他治疗的情况下,停用乌帕替尼一周后,患者恢复排便,肠梗阻症状改善,提示药物与肠梗阻之间可能存在关联,这被认为可能是由于Janus激酶抑制剂(JAKi)的脱靶效应所致。该病例说明了靶向治疗免疫调节作用的复杂性以及对其作用机制和副作用进行长期观察的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa90/11648534/b1b71cc04131/CCID-17-2855-g0001.jpg

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