Sirufo Maria Maddalena, De Martinis Massimo, Ginaldi Lia
Department of Life, Health and Environmental Sciences, University of L'Aquila Allergy an Clinical Immunology Unit, AUSL Teramo, Italy.
Medicine (Baltimore). 2018 Jun;97(24):e10897. doi: 10.1097/MD.0000000000010897.
Atopic dermatitis is a frequent, relapsing, chronic inflammatory skin condition with a deep negative impact on quality of life. Three are the major pathological factors driving its complex pathogenesis: the skin barrier disruption, the altered Th2 cell response and itching. Current management of the disease is often unsatisfactory, unable to induce a complete resolution of signs and symptoms or at least a significant clinical improvement with adequate patient satisfaction.
We report the case of a 57-year-old man with severe chronic atopic dermatitis for at least 40 years irresponsive to traditional therapies. The patient was treated in the past with different standard therapeutic regimens without satisfactory and lasting results.
The diagnosis of AD was based on the revised criteria of Hanifin and Rjika and the Scoring Atopic Dermatitis was assessed together with laboratory evaluation.
He received off-label omalizumab (300 mg subcutaneous injection repeated at 2-week intervals for six months).
Scorad and laboratory findings were assessed montly and demonstrated a progressive decrease (SCORAD and ECP levels) togheter with general clinical improvement. Omalizumab, in our patient, determined a significant symptomatic improvement, assessed by SCORAD, simultaneously with a progressive decline in ECP serum levels, whit no side effects, confirming the substantial safety of the drug.
The satisfactory response to omalizumab after the failure of all previous traditional treatments, confirms the efficacy of this biological drug in the therapy of refractory AD with high IgE levels and increased ECP serum levels. The lesson learnt from this case report is that Omalizumab represent an effective and safe alternative to traditional therapies in patients with severe irresponsive atopic dermatitis.
特应性皮炎是一种常见的、复发性的慢性炎症性皮肤病,对生活质量有严重负面影响。有三个主要病理因素驱动其复杂的发病机制:皮肤屏障破坏、Th2细胞反应改变和瘙痒。目前该疾病的治疗往往不尽人意,无法完全消除体征和症状,或者至少无法实现显著的临床改善并让患者获得足够的满意度。
我们报告了一例57岁男性患者,患有严重慢性特应性皮炎至少40年,对传统疗法无反应。该患者过去接受过不同的标准治疗方案,但均未取得满意且持久的效果。
特应性皮炎的诊断基于Hanifin和Rjika的修订标准,并结合实验室评估对特应性皮炎评分进行评估。
他接受了超说明书使用的奥马珠单抗治疗(皮下注射300mg,每2周重复一次,共6个月)。
每月评估Scorad和实验室检查结果,结果显示(Scorad和嗜酸性粒细胞阳离子蛋白水平)逐渐下降,同时整体临床状况有所改善。在我们的患者中,奥马珠单抗通过Scorad评估显示出显著的症状改善,同时嗜酸性粒细胞阳离子蛋白血清水平逐渐下降,且无副作用,证实了该药物的高度安全性。
在之前所有传统治疗均失败后,奥马珠单抗取得了令人满意的反应,证实了这种生物药物在治疗高IgE水平和嗜酸性粒细胞阳离子蛋白血清水平升高的难治性特应性皮炎中的疗效。从该病例报告中学到的经验是,对于严重难治性特应性皮炎患者,奥马珠单抗是传统疗法的一种有效且安全的替代方案。