Do Carmo Ana Paula, Battle Amanda R, Fragnan Nyla T Melo Lobao, Machado Carlos A S, Constantino-Silva Rosemeire N, Henrickson Sarah E, Grumach Anete S
Faculdade de Medicina, Centro Universitario FMABC, Santo Andre, SP, Brazil.
Discipline of Immunology, Faculdade de Medicina, Centro Universitario FMABC, Santo Andre, SP, Brazil.
Acta Derm Venereol. 2025 Jun 9;105:adv41318. doi: 10.2340/actadv.v105.41318.
Inborn errors of immunity are rare diseases and 50-80% present with dermatological manifestations. This study evaluated difficult-to-treat cutaneous human papillomavirus infections and their associations with immunological defects. Patients were recruited from the Dermatological Outpatient Clinic over 2 years. Patients reporting persistent common warts and/or a combination of molluscum contagiosum or more than 2 flat warts, with a clinical assessment of severe or persistent skin infection, met the clinical severity criteria for inclusion. Resistance to several therapies was also considered. A total of 632 patient records were analysed to clinically characterize the warts, laboratory data, treatments used and their responses, comorbidities, and family history. Among these, 459 cases were initially excluded from further evaluation. A questionnaire was provided by phone to 173 patients, among whom 47 patients were selected for an in-person consultation. Of these, 6 met the criteria for further evaluation. Immunological tests revealed neutropenia, low levels of immunoglobulin isotypes (IgA, IgM, and IgG), and reduced frequency of lymphocyte subsets. Family history, flat warts, and associated recurrent viral infections suggested the need for further immunological evaluation. Criteria are proposed for identifying patients with cutaneous warts that warrant additional evaluation for potential inborn errors of immunity.
遗传性免疫缺陷病是罕见病,50%-80%的患者有皮肤表现。本研究评估了难治性皮肤人乳头瘤病毒感染及其与免疫缺陷的关联。在两年多的时间里,从皮肤科门诊招募患者。报告有持续性寻常疣和/或传染性软疣合并存在或超过2个扁平疣,且临床评估为严重或持续性皮肤感染的患者,符合纳入的临床严重程度标准。对多种治疗方法的抵抗性也在考虑范围内。共分析了632份患者记录,以对疣进行临床特征分析、实验室数据、所用治疗方法及其反应、合并症和家族史进行分析。其中,459例最初被排除在进一步评估之外。通过电话向173例患者发放了问卷,其中47例患者被选来进行面诊。在这些患者中,6例符合进一步评估标准。免疫检测显示中性粒细胞减少、免疫球蛋白同种型(IgA、IgM和IgG)水平降低以及淋巴细胞亚群频率降低。家族史、扁平疣和相关的复发性病毒感染提示需要进一步进行免疫评估。本文提出了一些标准,用于识别患有皮肤疣且有必要进一步评估是否存在潜在遗传性免疫缺陷病的患者。