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RF – Tildrakizumab 200 mg. Is Double Dosing Really a Window of Opportunity? Tildrakizumab 200mg。双倍剂量真的有机会吗?
IF 2.8 Q1 DERMATOLOGY Pub Date : 2025-12-08 DOI: 10.1016/j.ad.2025.104539
C. Llamas-Segura , M. Cebolla-Verdugo , R. Ruiz-Villaverde
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引用次数: 0
Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis Induced by Topical Carbonic Anhydrase Inhibitors: A Literature Review 外用碳酸酐酶抑制剂诱导Stevens-Johnson综合征和中毒性表皮坏死松解:文献综述。
IF 2.8 Q1 DERMATOLOGY Pub Date : 2025-12-06 DOI: 10.1016/j.ad.2025.104528
L. Aguilar-González, G. Gallo-Pineda, I. Villegas-Romero, M. Viedma-Martínez
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引用次数: 0
A Rare Case of Acquired Reactive Perforating Collagenosis in a Child With Type 1 Diabetes 1型糖尿病儿童获得性反应性穿孔性胶原沉积1例。
IF 2.8 Q1 DERMATOLOGY Pub Date : 2025-12-06 DOI: 10.1016/j.ad.2025.104527
R.P. Román Cheuque, D. Jiménez-Gallo, I. Villegas Romero, M. Linares Barrios
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引用次数: 0
Safety and Efficacy of Bimekizumab in Patients With Moderate-to-Severe Hidradenitis Suppurativa: A Multicenter Retrospective Cohort Study 比美珠单抗治疗中重度化脓性汗腺炎的安全性和有效性:一项多中心回顾性队列研究
IF 2.8 Q1 DERMATOLOGY Pub Date : 2025-12-05 DOI: 10.1016/j.ad.2025.104531
M. Mansilla-Polo , M. Pons-Benavent , P. Fernández-Crehuet , E. Vilarrasa , C. Albanell-Fernández , E. Morales-Tedone , F. Rausell-Félix , R. Alcalá-García , M. Matellanes-Palacios , G. Martín-Ezquerra , F. Alfageme , C. Ciudad-Blanco , M.T. López-Villaescusa , J.M. Segura-Palacios , J.C. Pascual-Ramírez , M.L. Fernández-Díaz , D. Falkenhain-López , M. García-Gil , A. Agustí-Mejías , N. No-Pérez , A. Molina-Leyva

Background

Bimekizumab is the first and only dual selective inhibitor of IL-17 A and IL-17 F that has been proven effective and safe in Phase 3 clinical trials and has been approved by the European Medicines Agency (EMA) for the treatment of hidradenitis suppurativa (HS).

Objectives

To assess the safety and efficacy profile of bimekizumab in patients with moderate-to-severe HS across multiple centers in Spain.

Methods

We conducted a retrospective cohort study including 84 patients treated with bimekizumab. Efficacy was assessed using an intention-to-treat approach, with patients who discontinued treatment for any reason or were lost to follow-up considered nonresponders. Data were collected at baseline, week 16, and week 24.

Results

The analysis included a total of 84 patients at 16 weeks, with 43 having completed the 24-week follow-up assessment (56 men [66.67%] and 28 women [33.33%]) with a mean age of 44.17 (13.43) years and a mean baseline IHS4 of 23.75 (12.87) were included. By week 24, IHS4 scores dropped by 16.73 points (p < 0.0001); a HiSCR50 of 55.95% was achieved at week 16, which was maintained with a HiSCR50 of 55.81% at week 24; DLQI scores improved by 10.67 points (p < 0.0001); pain scores dropped by 3.42 points (p < 0.0001); and flare counts were reduced by 1.53 (p = 0.0006). Adverse events were reported in 20.24% of patients by week 16, mainly candidiasis, and dropped to 11.90% by week 24. 53.57% (45/84) of patients achieved IHS4-55 by week 16, and by week 24, 60.47% (26/43) of patients maintained or reached this response level.

Conclusions

Bimekizumab is effective for the treatment of HS in real-world clinical practice, with a manageable safety profile over the 24-week period. Our findings are consistent with those reported in phase 3 clinical trials.
背景:Bimekizumab是第一个也是唯一一个在iii期临床试验中被证明有效和安全的IL-17 A和IL-17 F双选择性抑制剂,并已被欧洲药品管理局(EMA)批准用于治疗化脓性汗腺炎(HS)。目的:评估比美珠单抗在西班牙多个中心治疗中重度HS患者的安全性和有效性。方法:我们进行了一项回顾性队列研究,包括84例接受比美珠单抗治疗的患者。使用意向治疗方法评估疗效,因任何原因停止治疗或失去随访的患者被认为无反应。在基线、第16周和第24周收集数据。结果:16周时共纳入84例患者,其中43例完成了24周的随访评估(男性56例[66.67%],女性28例[33.33%]),平均年龄44.17(13.43)岁,平均基线IHS4为23.75(12.87)。到第24周,IHS4评分下降16.73分(p < 0.0001);在第16周达到55.95%的HiSCR50,在第24周保持55.81%;DLQI评分提高10.67分(p < 0.0001);疼痛评分下降3.42分(p < 0.0001);耀斑计数减少1.53 (p = 0.0006)。第16周不良事件发生率为20.24%,以念珠菌感染为主,第24周不良事件发生率下降至11.90%。到第16周,53.57%(45/84)的患者达到IHS4-55,到第24周,60.47%(26/43)的患者维持或达到该应答水平。结论:在现实世界的临床实践中,Bimekizumab治疗HS是有效的,在24周的时间内具有可控的安全性。我们的发现与三期临床试验报告一致。
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引用次数: 0
Practical Approach to Direct Visualization of Methylene Blue-stained Urethral Specimens in Cases of Symptomatic Urethritis 有症状性尿道炎病例亚甲基蓝染色尿道标本直接可视化的实用方法。
IF 2.8 Q1 DERMATOLOGY Pub Date : 2025-12-05 DOI: 10.1016/j.ad.2025.104536
A. Fernández-Galván , M. Seguí-Olmedilla , F.J. Bru-Gorraiz , A. Martin-Gorgojo
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引用次数: 0
Irregular Globular Ridge Pattern in Acral Melanoma 肢端黑色素瘤的不规则球形脊型。
IF 2.8 Q1 DERMATOLOGY Pub Date : 2025-12-05 DOI: 10.1016/j.ad.2025.104535
I.M. Coronel-Pérez , D. Casado-Gómez , L. Pedraza-Gil
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引用次数: 0
Incidental Adnexal Neoplasm at an Uncommon Site 罕见部位偶发的附件肿瘤。
IF 2.8 Q1 DERMATOLOGY Pub Date : 2025-12-04 DOI: 10.1016/j.ad.2025.104513
M. Fernández-Parrado , P. Rodríguez-Jiménez , A. Pasco-Peña
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引用次数: 0
Male-pattern Androgenetic Alopecia in Women on Hormonal Treatment: Further Evidence for a Dual Male–Female Pathogenic Mechanism 激素治疗的女性男性型雄激素性脱发:男性-女性双重致病机制的进一步证据。
IF 2.8 Q1 DERMATOLOGY Pub Date : 2025-12-04 DOI: 10.1016/j.ad.2025.104523
A. Fernandez-Flores , J. García Silva
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引用次数: 0
Management of Immune-Mediated Alopecia With Tumor Necrosis Factor Alpha Inhibitors: A Report of 4 Cases 肿瘤坏死因子α抑制剂治疗免疫介导性脱发(附4例报告)
IF 2.8 Q1 DERMATOLOGY Pub Date : 2025-12-04 DOI: 10.1016/j.ad.2025.104510
P. Villodre Lozano, Á. Aguado Vázquez, C. Alonso Díez, A. Mateu Puchades
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引用次数: 0
Mortality Outcomes in Patients With Plaque Psoriasis and Hidradenitis Suppurativa: The Role of Biologic Therapy 斑块型银屑病和化脓性汗腺炎患者的死亡率:生物治疗的作用。
IF 2.8 Q1 DERMATOLOGY Pub Date : 2025-12-04 DOI: 10.1016/j.ad.2025.104525
R. Rivera-Díaz , B. Joven , A. Gotor-Rivera , J. Hernández

Background and objectives

Plaque psoriasis (Pso) and hidradenitis suppurativa (HS) are chronic inflammatory diseases associated with multiple comorbidities, including cardiovascular conditions, which may negatively impact survival. The aim of this study was to analyze mortality in patients with Pso and HS vs the general population and to each other, as well as the potential impact of biologic therapy on mortality.

Materials and methods

We conducted a retrospective cohort study based on electronic health records retrieved from the TriNetX platform. Patients diagnosed with Pso or HS, with or without biologic therapy, were compared with matched cohorts from the general population and with each other. Cohorts were matched using propensity score matching (PSM) and adjusted for age, sex, and comorbidities potentially affecting mortality, including smoking, diabetes, hyperlipidemia, hypertension, overweight and obesity, cardiovascular disease, pulmonary embolism, venous thrombosis, ischemic heart disease, and cerebrovascular disease. The mortality incidence rate was assessed using risk ratio (RR) and hazard ratio (HR), with 95% confidence intervals (CIs) during a 10-year follow-up.

Results

After adjustment, 76,191 patients with Pso and 52,354 with HS were included. Compared to the general population, patients with Pso showed a higher mortality risk (RR, 2.25; 95%CI, 2.18–2.32; HR, 2.02; 95%CI, 1.95–2.08), with a significant reduction in those treated with biologics (RR, 0.76; 95%CI, 0.70–0.83; HR, 0.62; 95%CI, 0.57–0.67). Similarly, patients with HS also exhibited a higher mortality risk (RR, 2.25; 95%CI, 2.14–2.37; HR, 2.28; 95%CI, 2.16–2.40), which was attenuated in those treated with biologics (RR, 0.80; 95%CI, 0.65–0.99; HR, 0.62; 95%CI, 0.49–0.77). When comparing both diseases, patients with HS had a higher mortality risk vs those with Pso (HR, 1.16; 95%CI, 1.11–1.22). The same trend was observed in biologic-treated subgroups (RR, 1.30; 95%CI, 1.00–1.68; HR, 1.45; 95%CI, 1.12–1.90).

Conclusions

Both psoriasis (pso) and hidradenitis suppurativa (hs) are associated with an increased risk of mortality, which appears to be mitigated by biologic therapy. Early and comprehensive management of these conditions, including systemic inflammation control and comorbidity screening, may improve survival outcomes.
背景和目的:斑块型银屑病(Pso)和化脓性汗腺炎(HS)是慢性炎症性疾病,伴有多种合并症,包括心血管疾病,可能对生存产生负面影响。本研究的目的是分析Pso和HS患者与一般人群的死亡率,以及相互之间的死亡率,以及生物治疗对死亡率的潜在影响。材料和方法:我们基于从TriNetX平台检索的电子健康记录进行了一项回顾性队列研究。诊断为Pso或HS的患者,接受或不接受生物治疗,与来自一般人群的匹配队列进行比较,并相互比较。使用倾向评分匹配(PSM)对队列进行匹配,并根据年龄、性别和可能影响死亡率的合并症进行调整,包括吸烟、糖尿病、高脂血症、高血压、超重和肥胖、心血管疾病、肺栓塞、静脉血栓形成、缺血性心脏病和脑血管疾病。在10年随访期间,采用风险比(RR)和危险比(HR)评估死亡率,95%置信区间(ci)。结果:经调整后,共纳入Pso患者76.191例,HS患者52.354例。与一般人群相比,Pso患者的死亡风险较高(RR, 2.25; 95%CI, 2.18-2.32; HR, 2.02; 95%CI, 1.95-2.08),而接受生物制剂治疗的患者死亡率显著降低(RR, 0.76; 95%CI, 0.70-0.83; HR, 0.62; 95%CI, 0.57-0.67)。同样,HS患者也表现出较高的死亡风险(RR, 2.25; 95%CI, 2.14-2.37; HR, 2.28; 95%CI, 2.16-2.40),而接受生物制剂治疗的患者死亡率降低(RR, 0.80; 95%CI, 0.65-0.99; HR, 0.62; 95%CI, 0.49-0.77)。当比较两种疾病时,HS患者的死亡风险高于Pso患者(HR, 1.16; 95%CI, 1.11-1.22)。在生物处理亚组中观察到同样的趋势(RR, 1.30; 95%CI, 1.00-1.68; HR, 1.45; 95%CI, 1.12-1.90)。结论:银屑病(pso)和化脓性汗腺炎(hs)都与死亡风险增加相关,生物治疗似乎可以减轻这种风险。对这些疾病进行早期和全面的管理,包括全身性炎症控制和合并症筛查,可能会改善生存结果。
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Actas dermo-sifiliograficas
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