Brenda Guendulain-Velázquez, Patricia María O'Farrill-Romanillos
{"title":"[常见变异性免疫缺陷病患者的皮肤病表现]。","authors":"Brenda Guendulain-Velázquez, Patricia María O'Farrill-Romanillos","doi":"10.29262/ram.v71i2.1296","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Estimate the prevalence of dermatological manifestations in Mexican patients with common variable immunodeficiency.</p><p><strong>Methods: </strong>Cross-sectional and retrospective study, based on the analysis of records of patients with a diagnosis of common variable immunodeficiency, treated at the Siglo XXI National Medical Center (Mexican Social Security Institute), according to the criteria of the European Society of Immunodeficiencies (ESID). and of which only 3 had a genetic diagnosis with the following mutations: IRF2, CTLA4 and PIK-3, belonging to the Immunodeficiency Clinic of the National Medical Center Siglo XXI (IMSS), to evaluate dermatological manifestations, review of laboratory tests: IgA, IgM, IgG and type of replacement therapy with Immunoglobulin. The statistical analysis was carried out with the SPSS program; Descriptive statistics were used to analyze the data, according to the type of variable to be analyzed.</p><p><strong>Results: </strong>36 patients were included, of which 55.5% were women; with median age 34 years (18-94). The prevalence of dermatological manifestations was 70% (n = 25). 30.5% had a history of infectious dermatosis and 39.5% had a history of non-infectious dermatosis. The most common dermatosis was irritant contact dermatitis in 13.8% of patients. All received replacement therapy with human immunoglobulin, 33.3% intravenously and the rest subcutaneously.</p><p><strong>Conclusions: </strong>Common variable immunodeficiency is an inborn error of immunity, with different clinical manifestations in various organs and systems (the skin is one of these). Dermatological manifestations are not usually described in patients with common variable immunodeficiency; However, it is important to identify them due to their relationship with certain complications (increased risk of superinfection), due to skin disruption and biological therapies.</p>","PeriodicalId":101421,"journal":{"name":"Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993)","volume":"71 2","pages":"91-95"},"PeriodicalIF":0.0000,"publicationDate":"2024-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Prevalence of dermatological manifestations in common variable immunodeficiency patients].\",\"authors\":\"Brenda Guendulain-Velázquez, Patricia María O'Farrill-Romanillos\",\"doi\":\"10.29262/ram.v71i2.1296\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Estimate the prevalence of dermatological manifestations in Mexican patients with common variable immunodeficiency.</p><p><strong>Methods: </strong>Cross-sectional and retrospective study, based on the analysis of records of patients with a diagnosis of common variable immunodeficiency, treated at the Siglo XXI National Medical Center (Mexican Social Security Institute), according to the criteria of the European Society of Immunodeficiencies (ESID). and of which only 3 had a genetic diagnosis with the following mutations: IRF2, CTLA4 and PIK-3, belonging to the Immunodeficiency Clinic of the National Medical Center Siglo XXI (IMSS), to evaluate dermatological manifestations, review of laboratory tests: IgA, IgM, IgG and type of replacement therapy with Immunoglobulin. The statistical analysis was carried out with the SPSS program; Descriptive statistics were used to analyze the data, according to the type of variable to be analyzed.</p><p><strong>Results: </strong>36 patients were included, of which 55.5% were women; with median age 34 years (18-94). The prevalence of dermatological manifestations was 70% (n = 25). 30.5% had a history of infectious dermatosis and 39.5% had a history of non-infectious dermatosis. The most common dermatosis was irritant contact dermatitis in 13.8% of patients. All received replacement therapy with human immunoglobulin, 33.3% intravenously and the rest subcutaneously.</p><p><strong>Conclusions: </strong>Common variable immunodeficiency is an inborn error of immunity, with different clinical manifestations in various organs and systems (the skin is one of these). Dermatological manifestations are not usually described in patients with common variable immunodeficiency; However, it is important to identify them due to their relationship with certain complications (increased risk of superinfection), due to skin disruption and biological therapies.</p>\",\"PeriodicalId\":101421,\"journal\":{\"name\":\"Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993)\",\"volume\":\"71 2\",\"pages\":\"91-95\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-06-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.29262/ram.v71i2.1296\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29262/ram.v71i2.1296","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
目的估计墨西哥常见可变免疫缺陷病患者皮肤病的发病率:根据欧洲免疫缺陷协会(ESID)的标准,对在 Siglo XXI 国家医疗中心(墨西哥社会保障局)接受治疗并确诊为常见可变免疫缺陷患者的记录进行分析:IRF2、CTLA4 和 PIK-3,隶属于国家二十一世纪医疗中心(IMSS)的免疫缺陷诊所,以评估皮肤病表现,审查实验室检测结果:IgA、IgM、IgG 和免疫球蛋白替代疗法的类型。统计分析使用 SPSS 程序进行;根据待分析变量的类型,使用描述性统计对数据进行分析:共纳入 36 名患者,其中 55.5% 为女性,中位年龄为 34 岁(18-94 岁)。皮肤病的发病率为 70%(25 人)。30.5%的患者有感染性皮肤病病史,39.5%的患者有非感染性皮肤病病史。最常见的皮肤病是刺激性接触性皮炎,占患者总数的 13.8%。所有患者都接受了人免疫球蛋白替代治疗,其中33.3%的患者接受静脉注射,其余患者接受皮下注射:结论:常见变异性免疫缺陷是一种先天性免疫缺陷,在不同器官和系统(皮肤就是其中之一)有不同的临床表现。常见可变免疫缺陷症患者通常不会出现皮肤表现;然而,由于皮肤破坏和生物疗法会导致某些并发症(增加超级感染的风险),因此识别皮肤表现非常重要。
[Prevalence of dermatological manifestations in common variable immunodeficiency patients].
Objective: Estimate the prevalence of dermatological manifestations in Mexican patients with common variable immunodeficiency.
Methods: Cross-sectional and retrospective study, based on the analysis of records of patients with a diagnosis of common variable immunodeficiency, treated at the Siglo XXI National Medical Center (Mexican Social Security Institute), according to the criteria of the European Society of Immunodeficiencies (ESID). and of which only 3 had a genetic diagnosis with the following mutations: IRF2, CTLA4 and PIK-3, belonging to the Immunodeficiency Clinic of the National Medical Center Siglo XXI (IMSS), to evaluate dermatological manifestations, review of laboratory tests: IgA, IgM, IgG and type of replacement therapy with Immunoglobulin. The statistical analysis was carried out with the SPSS program; Descriptive statistics were used to analyze the data, according to the type of variable to be analyzed.
Results: 36 patients were included, of which 55.5% were women; with median age 34 years (18-94). The prevalence of dermatological manifestations was 70% (n = 25). 30.5% had a history of infectious dermatosis and 39.5% had a history of non-infectious dermatosis. The most common dermatosis was irritant contact dermatitis in 13.8% of patients. All received replacement therapy with human immunoglobulin, 33.3% intravenously and the rest subcutaneously.
Conclusions: Common variable immunodeficiency is an inborn error of immunity, with different clinical manifestations in various organs and systems (the skin is one of these). Dermatological manifestations are not usually described in patients with common variable immunodeficiency; However, it is important to identify them due to their relationship with certain complications (increased risk of superinfection), due to skin disruption and biological therapies.