中国麻风皮肤病杂志 ›› 2026, Vol. 42 ›› Issue (3): 206-210.doi: 10.12144/zgmfskin202603206

• 临床研究 • 上一篇    下一篇

乌帕替尼治疗度普利尤单抗相关甲银屑病一例并文献复习

邵玉玲1,2,王娜1,2   

  1. 1山东第一医科大学附属皮肤病医院,山东济南,250022;2山东省皮肤病性病防治研究所,山东济南,250022
  • 出版日期:2026-03-15 发布日期:2026-03-10

Successful treatment of dupilumab-associated nail psoriasis with upadacitinib: a case report and literature review

SHAO Yuling1,2, WANG Na1,2   

  1. 1 Dermatology Hospital of Shandong First Medical University, Jinan 250022, China; 2 Shandong Provincial Institute of Dermatology and Venereology, Shandong Academy of Medical Sciences, Jinan 250022, China
  • Online:2026-03-15 Published:2026-03-10

摘要: 患者,女,53岁。1年前外院诊断为特应性皮炎并给予度普利尤单抗治疗,共治疗9次,随后患者躯干、四肢出现鳞屑性红斑、丘疹伴瘙痒。我院皮损组织病理检查示银屑病,进一步追问病史,患者有银屑病个人史及家族史,遂给予环孢素治疗,4个月后皮损逐渐消退。减停环孢素期间,患者双手指甲出现增厚、混浊伴疼痛,辅助检查:IGRA及PDD试验阳性。诊断:甲银屑病;结核潜伏感染。患者预防性抗结核治疗1个月后,给予乌帕替尼缓释片治疗,2个月后甲损害明显改善,4个月后指甲恢复正常。随访期间无新发银屑病皮损及药物不良反应发生。此外,本文对相关文献进行总结,探讨度普利尤单抗诱发银屑病的可能机制、甲银屑病的治疗选择及乌帕替尼在难治性甲银屑病中治疗的优势及注意事项。

关键词: 特应性皮炎, 银屑病, 度普利尤单抗, JAK抑制剂, 乌帕替尼

Abstract: A 53-year-old female patient was diagnosed with atopic dermatitis in another hospital one year prior and received dupilumab therapy for a total of nine administrations. Subsequently, scaly erythema, papules accompanied by pruritus emerged on her trunk and extremities. Pathological examination of the skin lesions in our hospital confirmed psoriasis. Further inquiry about her medical history revealed a personal and familial history of psoriasis. After a confirmed diagnosis of psoriasis, she was treated with cyclosporine for four months, and the skin lesions gradually subsided. During the tapering and discontinuation of cyclosporine, the patient developed thickening, opacity and pain in the nails of both hands. Auxiliary examinations showed positive for interferon-gamma release assay (IGRA) and purified protein derivative (PPD) skin test. The final diagnoses were nail psoriasis and latent tuberculosis infection (LTBI).One month after initiating preventive anti-tuberculosis treatment, the patient was prescribed upadacitinib extended-release tablets. Two months later, significant improvement was observed in the nail lesions; after four months of treatment, the nails returned to normal. During the follow-up period, no new psoriatic lesions or adverse drug reactions occurred. In addition, this paper summarizes relevant literature and discusses the potential mechanisms of dupilumab-induced psoriasis, therapeutic options for nail psoriasis, as well as the advantages and precautions of upadacitinib in the management of refractory nail psoriasis.

Key words: atopic dermatitis, psoriasis, dupilumab, JAK inhibitor, upadacitinib