Qiu Miaoqi, Man Xiaoyong, Jing Jing
Department of Dermatology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, People's Republic of China.
J Inflamm Res. 2025 May 29;18:6959-6961. doi: 10.2147/JIR.S504393. eCollection 2025.
Dissecting Cellulitis of the Scalp (DCS) is a rare form of neutrophilic primary cicatricial alopecia (PCA). It usually occurs in black males and is less commonly reported in Asian populations. There are no systematic treatment guidelines for this disease, the hypothetical co-pathogenesis of DCS and hidradenitis suppurativa (HS) has led to the fact that most of the current biological therapies for DCS are based on the experience of HS, such as biologics and JAK inhibitors. Both agents alone have been reported in the treatment of HS and DCS, but the efficacy is uncertain. For severely refractory DCS, the combination of biologics and Janus kinase inhibitors (JAKi) may be a new strategy. In this case, we describe a 28-year-old Chinese young man with a confirmed diagnosis of severe DCS who experienced nodules resolve and hair regrowth after a combination use of ixekizumab and tofacitinib. This is the first case of DCS treated with a combination of IL-17 inhibitors and JAKi.
We hope that dermatologists should be aware that early diagnosis of DCS and the application of biologics are essential to quickly control symptoms and prevent from PCA and keloids.
This is a patient from the Department of Dermatology, the Second Affiliated Hospital of Zhejiang University School of Medicine.
头皮穿掘性蜂窝织炎(DCS)是一种罕见的嗜中性粒细胞性原发性瘢痕性脱发(PCA)。它通常发生在黑人男性中,在亚洲人群中报道较少。对于这种疾病没有系统的治疗指南,DCS与化脓性汗腺炎(HS)的假设共同发病机制导致目前大多数针对DCS的生物疗法都是基于HS的经验,如生物制剂和JAK抑制剂。这两种药物单独使用都曾被报道用于治疗HS和DCS,但疗效不确定。对于严重难治性DCS,生物制剂和Janus激酶抑制剂(JAKi)联合使用可能是一种新策略。在此病例中,我们描述了一名确诊为重度DCS的28岁中国青年男性,在联合使用司库奇尤单抗和托法替布后结节消退且毛发再生。这是首例使用IL-17抑制剂和JAKi联合治疗DCS的病例。
我们希望皮肤科医生应意识到,DCS的早期诊断和生物制剂的应用对于快速控制症状以及预防PCA和瘢痕疙瘩至关重要。
这是一名来自浙江大学医学院附属第二医院皮肤科的患者。