Farahnik Benjamin, Beroukhim Kourosh, Nakamura Mio, Abrouk Michael, Zhu Tian Hao, Singh Rasnik, Lee Kristina, Bhutani Tina, Koo John, Liao Wilson
University of Vermont College of Medicine, Burlington, Vermont.
Dermatol Online J. 2017 May 15;23(5):13030/qt3588p0hn.
Atopic dermatitis (AD) is a common inflammatory dermatosis characterized by pruritus, erythema, induration, and lichenification. Current treatment options for generalized atopic dermatitis are limited and have potentially serious adverse effects, especially in patients with severe, chronic AD who frequently require systemic anti-inflammatory agents. Apremilast, an oral phosphodiesterase-4 inhibitor, was FDA approved in September 2014 for the treatment of moderate-to-severe plaque psoriasis. However, its upstream anti-inflammatory effects, ease of use as an oral agent, and mild side-effect profile make it an interesting treatment option for AD as well. Herein, we present a patient with a life-long history of AD recalcitrant to topical steroids and cyclosporine who attained subjective and objective improvement in pruritus and erythema after 10-week treatment with apremilast.
特应性皮炎(AD)是一种常见的炎症性皮肤病,其特征为瘙痒、红斑、硬结和苔藓样变。目前针对泛发性特应性皮炎的治疗选择有限,且具有潜在的严重不良反应,尤其是在重度、慢性AD患者中,这些患者经常需要使用全身性抗炎药物。阿普米司特是一种口服磷酸二酯酶-4抑制剂,于2014年9月获得美国食品药品监督管理局(FDA)批准用于治疗中度至重度斑块状银屑病。然而,其上游抗炎作用、作为口服药物的易用性以及轻微的副作用 profile 使其也成为AD的一个有吸引力的治疗选择。在此,我们报告一名有AD终身病史、对局部类固醇和环孢素治疗无效的患者,在用阿普米司特治疗10周后,其瘙痒和红斑在主观和客观上均有改善。