Di Lernia Vito, Peccerillo Francesca
Dermatology Unit, Azienda Unità Sanitaria Locale- IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Clin Cosmet Investig Dermatol. 2024 Oct 15;17:2297-2300. doi: 10.2147/CCID.S483166. eCollection 2024.
Pityriasis rubra pilaris (PRP) is a rare chronic inflammatory skin disease characterised by follicular keratotic papules and perifollicular erythema coalescing into orange-red scaly plaques, and palmoplantar keratoderma. Characteristic islands of sparing are usually observed. A standardised therapeutic approach is lacking owing to the infrequent occurrence of this disease. However, anti-interleukin (IL)-17 and anti-IL-23 therapies have recently emerged as effective therapies in patients affected by PRP, with improvements in severity scores, change in severity of erythema, scaling, and thickness of lesions. Here, we report a 43-year old, female breast cancer who developed severe refractory PRP, which greatly impacted her quality of life. The patient experienced a marked improvement after treatment with tildrakizumab. Treatment was stopped after one year, and the three-year follow-up did not show relapse. In conclusion, 52- week treatment with tildrakizumab, an IL-23 antagonist, proved to be a favourable treatment option for PRP, leading to good patient adherence, improvement in quality of life, and long-term follow-up without relapse.
红皮病型毛发红糠疹(PRP)是一种罕见的慢性炎症性皮肤病,其特征为毛囊角化性丘疹和毛囊周围红斑融合成橙红色鳞屑斑块,以及掌跖角化病。通常可见特征性的无皮疹区。由于这种疾病发病率低,缺乏标准化的治疗方法。然而,抗白细胞介素(IL)-17和抗IL-23疗法最近已成为治疗PRP患者的有效疗法,患者的严重程度评分有所改善,红斑、鳞屑和皮损厚度的严重程度也有所变化。在此,我们报告一名43岁的女性乳腺癌患者,她患上了严重难治性PRP,这极大地影响了她的生活质量。患者使用替拉珠单抗治疗后有明显改善。治疗一年后停药,三年随访未显示复发。总之,使用IL-23拮抗剂替拉珠单抗进行52周治疗被证明是PRP的一种良好治疗选择,可使患者良好依从,改善生活质量,并长期随访无复发。