用S-100和黑-45免疫染色评价白癜风活动期和稳定期

Gurpinder Kaur, R. Punia, R. Kundu, G. Thami
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引用次数: 2

摘要

背景:白癜风是世界范围内最常见的色素疾病。在大多数情况下,诊断仅由临床检查作出。需要评估疾病状态(活跃/稳定)以做出适当的治疗决定。目的:本研究的目的是评价活动性和稳定性病变的组织病理学和免疫组织化学特征。材料与方法:50例白癜风患者(临床活动性和稳定性各25例)白癜风区活检;苏木精和伊红染色,Masson Fontana (MF), S-100和human melanoma black-45 (HMB-45)染色切片。结果:患者年龄7 ~ 69岁,平均年龄33.6±15.73岁。50例患者中,男性27例(54%),女性23例(46%)。所有病例均表现不同程度的基底色素沉着。与稳定病变相比,活动性病变常见于表皮海绵状病变、基底空泡变性、真皮噬黑素细胞和真皮淋巴单核细胞。MF染色显示,23/25例(92%)活动性白癜风患者基底黑色素完全丧失。HMB-45免疫染色在稳定型和活动力型白癜风中显示黑色素细胞阳性的平均值分别为2.52±1.0/ hpf和0.08±0.28/hpf,而S-100免疫染色显示Langerhans细胞阳性的平均值分别为1.70±0.38/hpf和7.78±4.11/hpf。结论:免疫组化显示活动性白癜风病变中hmb -45阳性黑色素细胞数量总体减少,s -100阳性朗格汉斯树突状细胞数量总体增加。该技术在区分白癜风的活跃和稳定阶段具有巨大的帮助,从而指导治疗。
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Evaluation of active and stable stages of vitiligo using S-100 and human melanoma black-45 immunostains
Background: Vitiligo is the most prevalent pigmentary disorder occurring worldwide. In most cases, the diagnosis is made by clinical examination alone. The disease status (active/stable) needs to be assessed to make appropriate therapeutic decisions. Objective: The aim of the present study was to evaluate the histopathological and immunohistochemical features in active and stable lesions. Materials and Methods: Biopsies from vitiliginous areas from 50 patients (25 each of clinically active and stable vitiligo); with hematoxylin and eosin, Masson Fontana (MF), S-100, and human melanoma black-45 (HMB-45) stained sections were studied. Results: Age of the patients ranged from 7 to 69 years (mean age: 33.6 ± 15.73 years). Of 50 patients, 27 (54%) were male and 23 (46%) were female. All the cases showed variable degree of basal hypopigmentation. Histopathological findings, epidermal spongiosis, basal vacuolar degeneration, dermal melanophages, and dermal lymphomononuclear cells were commonly observed in active lesions as compared to the stable ones. On MF staining, 23/25 cases (92%) of active vitiligo showed complete loss of basal melanin. Quantitative analysis of HMB-45 immunostaining in stable and active vitiligo revealed mean number of positive melanocytes as 2.52 ± 1.0/high power field (hpf) and 0.08 ± 0.28/hpf, respectively, while on S-100 immunostaining the mean values of positive Langerhans cells were 1.70 ± 0.38/hpf and 7.78 ± 4.11/hpf, respectively. Conclusion: The demonstration of overall reduction in the number of HMB-45-positive melanocytes and increase in S-100-positive Langerhans dendritic cells in the active vitiligo lesions is facilitated by immunohistochemistry. The technique is of immense help in differentiating active and stable stages of vitiligo, thus guiding therapy.
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