Devani Drashti, Chakraborty Disha, De Abhishek
Dermatology, Community Health Center (CHC) Kuvadava, Rajkot, IND.
Dermatology, Sacramento Veterans Affairs (VA) Medical Center, Rancho Cordova, USA.
Cureus. 2024 Oct 3;16(10):e70780. doi: 10.7759/cureus.70780. eCollection 2024 Oct.
Dupilumab is the first US FDA-approved biologic for moderate to severe atopic dermatitis (AD) in adults and children of age more than six months. It is a fully monoclonal antibody that inhibits interleukin (IL)-4 and IL-13 signal transmission. The initial product monograph mentioned major side effects like hypersensitivity reactions and eye problems like conjunctivitis, dry eye, and keratitis. Persistent facial redness with dupilumab administration has been reported in the past, and itraconazole proved to be effective for its treatment. We report a case of adult AD, on treatment with dupilumab, experiencing dupilumab facial redness (DFR), giving a positive response to itraconazole. DFR is a recognized complication of dupilumab therapy for AD. Clinicians should maintain a high index of suspicion for DFR, especially in patients presenting with new-onset facial symptoms during dupilumab treatment. Itraconazole can be considered a standard therapy for DFR, given its efficacy and tolerability profile in this context.
度普利尤单抗是美国食品药品监督管理局(FDA)批准的首个用于治疗6个月以上成人和儿童中重度特应性皮炎(AD)的生物制剂。它是一种完全单克隆抗体,可抑制白细胞介素(IL)-4和IL-13信号传导。最初的产品说明书提到了主要的副作用,如过敏反应以及眼部问题,如结膜炎、干眼症和角膜炎。过去曾有报道,使用度普利尤单抗会导致面部持续发红,而伊曲康唑被证明对其治疗有效。我们报告了一例接受度普利尤单抗治疗的成年AD患者出现度普利尤单抗面部发红(DFR),并对伊曲康唑治疗产生阳性反应的病例。DFR是度普利尤单抗治疗AD的一种公认并发症。临床医生应高度怀疑DFR,尤其是在度普利尤单抗治疗期间出现新发面部症状的患者中。鉴于伊曲康唑在这种情况下的疗效和耐受性,可将其视为DFR的标准治疗方法。