Di Stefani Alessandro, Galluzzo Marco, Talamonti Marina, Chiricozzi Andrea, Costanzo Antonio, Chimenti Sergio
Department of Dermatology, University of Rome "Tor Vergata", Rome, Italy.
J Dermatol Case Rep. 2013 Mar 30;7(1):5-9. doi: 10.3315/jdcr.2013.1127.
Pityriasis rubra pilaris is a rare, chronic erythematous squamous disorder of unknown etiology. The disease is characterized initially by small follicular papules that coalesce into yellowish pink scaly plaques, palmoplantar keratoderma, diffuse furfuraceous scale of the scalp, and frequent progression to exfoliative erythroderma. Generally it is difficult to discern pityriasis rubra pilaris from other skin conditions but key-clinical features help in the diagnosis such as "islands" of spared skin within generalized erythroderma, follicular keratotic plugs, and an orange hue of the involved skin. Treatment options include topical vitamin D analogues, keratolytics, systemic acitretin, methotrexate, cyclosporine, azathioprine, fumaric acid esters, phototherapy, and anti-TNFα agents. Cases, of pityriasis rubra pilaris, successfully treated with a short-course ustekinumab therapy, have been reported.
We report a 31-year-old man with pityriasis rubra pilaris, refractory to conventional treatments, successfully treated with ustekinumab monotherapy for over 64 weeks. After failing conventional systemic agents (cyclosporine, aciretin and methotrexate), ustekinumab 45 mg has been prescribed, with the same dosing regimen as in psoriasis. The patient improved dramatically within 4 weeks of the first injection, with markedly less erythema and pruritus. Long-term control of the disease of the disease was achieved (64 weeks of treatment).
We report this case in order to show the striking and rapid efficacy of ustekinumab in reducing the signs and symptoms of the disease. Complete remission was achieved after the third injection, but also a long-term control of the disease. The therapy was well-tolerated in our patient and no adverse events occurred.
毛发红糠疹是一种病因不明的罕见慢性红斑鳞屑性疾病。该病最初的特征是小的毛囊丘疹,融合形成淡黄色粉红色鳞屑斑块、掌跖角化病、头皮弥漫性糠秕状鳞屑,且常进展为剥脱性红皮病。一般来说,很难将毛发红糠疹与其他皮肤疾病区分开来,但关键的临床特征有助于诊断,如泛发性红皮病中存在的“正常皮肤岛”、毛囊角化性栓子以及受累皮肤的橙色色调。治疗选择包括外用维生素D类似物、角质剥脱剂、系统性阿维A、甲氨蝶呤、环孢素、硫唑嘌呤、富马酸酯、光疗和抗TNFα药物。已有报道称,用短疗程优特克单抗治疗毛发红糠疹取得成功的病例。
我们报告一名31岁患有毛发红糠疹的男性,对传统治疗无效,采用优特克单抗单药治疗超过64周后成功治愈。在传统系统性药物(环孢素、阿维A和甲氨蝶呤)治疗失败后,开具了45mg优特克单抗,给药方案与治疗银屑病相同。患者在首次注射后4周内显著改善,红斑和瘙痒明显减轻。实现了疾病的长期控制(治疗64周)。
我们报告该病例是为了展示优特克单抗在减轻疾病体征和症状方面显著且快速的疗效。第三次注射后实现了完全缓解,同时也实现了疾病的长期控制。我们的患者对该治疗耐受性良好,未发生不良事件。