Costa Tomás, Rebelo Clarisse, Marques Pinto Gabriela, Duarte Bruno
Dermatology, Centro Hospitalar Universitário Lisboa Central, Lisbon, PRT.
Dermatology, Centro Hospitalar Universitário do Algarve, Faro, PRT.
Cureus. 2023 Jan 3;15(1):e33321. doi: 10.7759/cureus.33321. eCollection 2023 Jan.
Darier disease (DD) is an autosomal-dominant genodermatosis in which mutations in the ATP2A2 gene result in impaired intercellular adhesion and epidermal blistering. Treatment options usually rely on systemic retinoids, but a refractory disease is still a therapeutical challenge. Given the similarity of DD pathogenesis with Hailey-Hailey disease, concomitant treatment with low-dose-naltrexone (LDN) has been proposed. We present the case of a 34-year-old woman with a 20-year history of severe, biopsy-proven DD, previously treated with several unsuccessful topical and systemic treatments, including oral isotretinoin, cyclosporine, doxycycline, methotrexate, acitretin, and subcutaneous adalimumab. At presentation, she had widespread keratotic, crusted, brown papules on her trunk and proximal extremities. Treatment with oral LDN (4.5 mg/day in manipulated tablets) was then initiated while maintaining the current isotretinoin therapy. After three months, there was a nearly complete clearance of the lesions, and no adverse effects were reported.
达里埃病(DD)是一种常染色体显性遗传性皮肤病,其中ATP2A2基因突变导致细胞间粘附受损和表皮水疱形成。治疗选择通常依赖于系统性维甲酸,但难治性疾病仍然是一个治疗挑战。鉴于DD发病机制与黑利-黑利病相似,有人提出联合使用低剂量纳曲酮(LDN)进行治疗。我们报告了一名34岁女性的病例,她有20年严重DD病史,经活检证实,此前接受过多种局部和全身治疗均未成功,包括口服异维甲酸、环孢素、强力霉素、甲氨蝶呤、阿维A和皮下注射阿达木单抗。就诊时,她的躯干和近端肢体有广泛的角化、结痂褐色丘疹。随后开始口服LDN(制成的片剂,4.5毫克/天)治疗,同时维持当前的异维甲酸治疗。三个月后,皮损几乎完全消退,且未报告有不良反应。