Department of Dermatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Br J Dermatol. 2017 Dec;177(6):1732-1736. doi: 10.1111/bjd.15509. Epub 2017 Oct 1.
Patients with deficiency of interleukin-36 receptor antagonist (DITRA), due to mutation of IL36RN, exhibit psoriatic phenotypes, typically generalized pustular psoriasis (GPP). We report a paediatric patient with DITRA, whose cutaneous lesions varied from psoriasis vulgaris in infancy to annular pustular psoriasis with acute exacerbation to GPP at 13 years of age. Conventional systemic treatments for GPP, which include oral retinoids, ciclosporin and methotrexate, are controversial in paediatric cases, because of their adverse effects and uncertain long-term consequences. Granulocyte monocyte apheresis, a process associated with few adverse events, promptly controlled the GPP of our paediatric patient, and has potential as a suitable alternative treatment for paediatric patients with DITRA.
白细胞介素-36 受体拮抗剂缺陷(DITRA)患者由于 IL36RN 突变,表现出银屑病表型,通常为泛发性脓疱型银屑病(GPP)。我们报告了一例 DITRA 儿科患者,其皮肤病变从婴儿期寻常型银屑病到环状脓疱型银屑病伴急性加重,至 13 岁时发展为 GPP。由于其不良反应和不确定的长期后果,用于 GPP 的常规全身治疗,包括口服维 A 酸、环孢素和甲氨蝶呤,在儿科病例中存在争议。粒细胞单核细胞吸附术是一种与较少不良反应相关的过程,迅速控制了我们儿科患者的 GPP,并且作为一种适合 DITRA 儿科患者的替代治疗方法具有潜力。