皮肤病科
医学
结节性痒疹
相互交织的
特应性皮炎
氨苯砜
英夫利昔单抗
湿疹性皮炎
肢端皮炎
杜皮鲁玛
病理
肿瘤坏死因子α
免疫学
替代医学
疾病
作者
Peter Dimitrion,Maria L. Espinosa,Jesse Veenstra
出处
期刊:Case Reports
[BMJ]
日期:2025-07-01
卷期号:18 (7): e266247-e266247
标识
DOI:10.1136/bcr-2025-266247
摘要
This case describes a woman with a decades-long history of misdiagnosed eczematous dermatitis ultimately identified as subcorneal pustular dermatosis (SPD), a rare neutrophilic dermatosis. Initially treated unsuccessfully for presumed atopic dermatitis and prurigo nodularis with various immunomodulatory agents, including dupilumab and Janus kinase (JAK) inhibitors, the correct diagnosis was made only after the appearance of characteristic flaccid pustules in intertriginous areas. Histopathological analysis confirmed SPD, and following intolerance to initial treatment with dapsone, the patient experienced a dramatic and sustained clinical improvement with infliximab. This case highlights the diagnostic challenges posed by atypical presentations of SPD and supports the use of tumour necrosis factor-alpha (TNFα) inhibitors as a highly effective treatment option.
科研通智能强力驱动
Strongly Powered by AbleSci AI