David Geffen School of Medicine at UCLA, Los Angeles, California.
Division of Dermatology, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California.
Dermatol Ther. 2017 Nov;30(6). doi: 10.1111/dth.12559. Epub 2017 Oct 15.
Pityriasis rubra pilaris (PRP) is a rare, difficult to treat papulosquamous disorder that responds variably to retinoids and immunosuppression. Successful use of biologics for treating PRP has been described in the literature by case reports and a limited number of case series. To provide additional data, we retrospectively analyzed cases of PRP treated with biologics at our institution. We identified seven patients with a clear diagnosis of PRP treated with adalimumab, etanercept, and/or ustekinumab at our institution from January 1, 2014 to April 1, 2017. Six of seven patients had type I, adult acquired PRP, and one had type V atypical juvenile PRP. In response to tumor necrosis factor (TNF)-α inhibition, two patients had marked responses (>75% improvement in involved body surface area), while three patients failed to show any improvement on a TNF-α inhibitor. In two cases of PRP refractory to TNF-α inhibition, ustekinumab resulted in a partial response (<75% improvement) in one patient and no response in the other. Compared to other published data, our cohort was substantially more resistant to treatment with biologics, a finding which may provide valuable perspective for dermatologists managing refractory PRP in the future.
红糠疹(PRP)是一种罕见的、难以治疗的丘疹鳞屑性疾病,对类视黄醇和免疫抑制的反应各不相同。文献中有个案报告和少数病例系列描述了生物制剂治疗 PRP 的成功案例。为了提供更多的数据,我们回顾性地分析了在我院接受生物制剂治疗的 PRP 病例。我们从 2014 年 1 月 1 日至 2017 年 4 月 1 日在我院发现了 7 名明确诊断为 PRP 的患者,他们接受了阿达木单抗、依那西普和/或乌司奴单抗治疗。7 名患者中的 6 名患有 I 型、成人获得性 PRP,1 名患有 V 型非典型青少年 PRP。在对肿瘤坏死因子(TNF)-α抑制剂的反应中,2 名患者有明显反应(受累体表面积改善>75%),而 3 名患者对 TNF-α抑制剂没有任何改善。在 2 例对 TNF-α抑制剂难治的 PRP 中,乌司奴单抗在 1 例患者中产生部分反应(受累体表面积改善<75%),另 1 例患者无反应。与其他已发表的数据相比,我们的队列对生物制剂的治疗明显更具耐药性,这一发现可能为未来皮肤科医生治疗难治性 PRP 提供有价值的视角。