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首页> 外文期刊>Indian journal of dermatology, venereology and leprology >Clinical, demographic and immunopathological spectrum of subepidermal autoimmune bullous diseases at a tertiary center: A 1-year audit
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Clinical, demographic and immunopathological spectrum of subepidermal autoimmune bullous diseases at a tertiary center: A 1-year audit

机译:第三中心表皮下自身免疫性大疱性疾病的临床,人口统计学和免疫病理学范围:为期1年的审核

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Background: The subepidermal autoimmune bullous diseases are a subset of immunobullous diseases encountered less frequently in the Indian population. There is a paucity of data on the prevalence, demographic and clinicopathological spectrum of various subepidermal autoimmune bullous diseases from India. Aim: To determine the demographic and clinicopathological profile of subepidermal autoimmune bullous diseases in Indian patients, presenting to the Immunobullous Disease Clinic of Postgraduate Institute of Medical Education and Research, Chandigarh. Methods: Patients seen from November 2013 to November 2014 who fulfilled the preset diagnostic criteria of subepidermal autoimmune bullous diseases were identified from case records. Data regarding demographic characteristics, clinical profile, immunopathological findings and treatment were collected from the predesigned proforma. Results: Of 268 cases of autoimmune bullous diseases registered, 50 (18.7%) were subepidermal autoimmune bullous diseases. Bullous pemphigoid was most frequently seen in 20 (40%) cases, followed by dermatitis herpetiformis in 14 (28%), mucous membrane pemphigoid in 6 (12%), chronic bullous dermatosis of childhood / linear immunoglobulin A bullous dermatosis in 5 (10%), lichen planus pemphigoides in 3 (6%), pemphigoid gestationis and epidermolysis bullosa acquisita in 1 (2%) case each. None of the patients had bullous systemic lupus erythematosus. Limitations: We could not perform direct and indirect immunofluorescence using salt-split skin as a substrate and immunoblotting due to non-availability of these facilities. Therefore, misclassification of subepidermal autoimmune bullous diseases in some cases cannot be confidently excluded. Conclusion: Subepidermal autoimmune bullous diseases are not uncommon in Indian patients. Bullous pemphigoid contributes maximally to the burden of subepidermal autoimmune bullous diseases in India, similar to that in the West, although the proportion is lower and disease onset is earlier. Dermatitis herpetiformis was observed to have a higher prevalence in our population, compared to that in the West and the Far East countries. The prevalence of other subepidermal autoimmune bullous diseases is relatively low. Detailed immunofluorescence and immunoblotting studies on larger patient numbers would help better characterize the pattern of subepidermal autoimmune bullous diseases and their features in Indian patients.
机译:背景:表皮下自身免疫性大疱性疾病是免疫性疾病的一部分,在印度人群中较少见。关于印度各种表皮下自身免疫性大疱性疾病的患病率,人口统计学和临床​​病理学方面的数据很少。目的:确定印度患者表皮下自身免疫性大疱性疾病的人口统计学和临床​​病理学特征,并向昌迪加尔医学教育与研究研究生院免疫球菌疾病诊所介绍。方法:从病例记录中识别出2013年11月至2014年11月间符合表皮下自身免疫性大疱性疾病诊断标准的患者。有关人口统计学特征,临床资料,免疫病理学发现和治疗的数据均来自预先设计的形式表。结果:在登记的268例自身免疫性大疱性疾病中,有50例(18.7%)是表皮下自身免疫性大疱性疾病。大疱性天疱疮最常见20例(40%),其次是疱疹状皮炎14例(28%),粘膜天疱疮6例(12%),儿童慢性大疱性皮肤病/线性免疫球蛋白5例大疱性皮肤病(10 %),扁平苔藓天疱疮3例(6%),天疱疮天疱疮和大疱表皮松解1例(2%)。所有患者均未患有大疱性系统性红斑狼疮。局限性:由于无法使用盐分分离的皮肤作为底物并进行免疫印迹,因此我们无法进行直接和间接免疫荧光。因此,在某些情况下不能可靠地排除表皮下自身免疫性大疱性疾病的错误分类。结论:表皮下自身免疫性大疱性疾病在印度患者中并不罕见。在印度,与西方国家相似,大疱性天疱疮最大程度地促进了表皮下自身免疫性大疱性疾病的负担,尽管该比例较低且发病较早。与西方和远东国家相比,人们发现疱疹样皮炎在我们的人群中患病率更高。其他表皮下自身免疫性大疱性疾病的患病率相对较低。对更多患者进行详细的免疫荧光和免疫印迹研究将有助于更好地表征印度患者表皮下自身免疫性大疱性疾病的模式及其特征。

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