界面皮炎的临床和病理表现及其相关性研究

M. Neelima, Anitha Sunkara, Saritha Karre, Maluthu Devojee, Dharavath Kavitha
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引用次数: 0

摘要

界面皮炎是一个广义的术语,用于所有具有表皮基底细胞损伤和广泛的单核细胞浸润乳头状真皮的临床特征和组织学特征的病变,所有这些病变也称为地衣样皮肤病或“地衣样组织反应”(LTR)。本研究的目的是详细研究与界面皮炎相关的组织病理学结果。材料与方法:共对112例患者进行研究。本研究的材料包括2009-2011年期间在塞昆德拉巴德甘地医学院皮肤科临床诊断为界面皮炎的患者。结果:本研究中诊断为界面皮炎的112例临床诊断如下:以扁平苔藓最多44例(39.29%),其次为盘状红斑狼疮10例(8.93%)、白癜风10例(8.93%)、色素性扁平苔藓9例(8.04%)、多形性红斑9例(8.04%)、亚急性红斑狼疮6例(5.36%)、固定药疹6例(5.36%)、硬化性扁平苔藓6例(5.36%)、增生性扁平苔藓6例(5.36%)、线状扁平苔藓、毛状扁平苔藓、肉芽性扁平苔藓、大疱性扁平苔藓、萎缩性扁平苔藓1例(39.29%)。地衣淀粉样变及药物诱导的类地衣反应。结论:界面皮炎包括表皮基底细胞损伤,细胞凋亡,形成胶质和果子体,基底细胞水样变性,基底膜增厚,带状或斑片状炎症浸润包围皮表皮交界处和黑色素失禁
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Study of clinical and histopathological findings of interface dermatitis and its correlation
Interface dermatitis is a broad term used for all the lesions having clinical features and histological features of epidermal basal cell damage and extensive mononuclear cell infiltration in the papillary dermis, all these lesions are also known as lichenoid dermatosis or “Lichenoid tissue reaction” (LTR). The aim of the study was to study in detail histopathological findings associated with interface dermatitis. Materials and methods: a total of 112 cases were studied. Material for this study included patients who were clinically diagnosed as having interface Dermatitis from the Department of Dermatology, Gandhi Medical College, Secunderabad, during the period from 2009-2011. Results: clinical diagnosis of the 112 cases diagnosed as interface dermatitis in the present study were as follows: The maximum number of cases 44 (39.29 %) were those of Lichen Planus, followed by discoid lupus erythematosus 10 (8.93 %), vitiligo 10 (8.93 %), lichen planus pigmentosus 9 (8.04 %), erythema multiforme 9 (8.04 %), subacute lupus erythematosus 6 (5.36 %), fixed drug eruption 6 (5.36 %), lichen sclerosis et atrophicus 6 (5.36 %), hypertropic lichen planus 6 (5.36 %) and 1 case of linear lichen planus, lichen plano pilaris, lichen nitidus, bullous lichen planus, atrophic lichen planus, lichen amyloidosis, and drug induced lichenoid reaction. Conclusion: the interface dermatitis encompasses disease in which there is epidermal basal cell damage, apoptosis of the cell with formation of colloid & civatte bodies, hydropic degeneration of the basal cell, basement membrane thickening, band like or patchy inflammatory infiltrate hugging the dermoepidermal junction and melanin incontinence
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