Rao Roopa S, Patil Shankargouda, Majumdar Barnali, Oswal Rakesh G
Professor and Head, Department of Oral Pathology & Microbiology, Faculty of Dental Sciences, MS Ramaiah University of Applied Sciences, Bengaluru, Karnataka, India.
Associate Professor, Department of Oral Pathology & Microbiology, Faculty of Dental Sciences, MS Ramaiah University of Applied Sciences, Bengaluru, Karnataka, India.
J Int Oral Health. 2015 Mar;7(3):1-5.
Keratins are the most abundant proteins and are characteristic findings in many epithelial pathologies, making it a diagnostically important marker, both histopathologically and immunohistochemically. Since, immunohistochemistry is an expensive diagnostic tool, special stains to detect the degree of keratinization could serve as a faster and economic option. The aim of the present study was to compare the efficacy of special stains for keratin with standard hematoxylin and eosin stain (H and E). Objectives include: (i) To subject the diagnosed cases of keratin disorders to the selected special stains: Ayoub-shklar method, Dane-Herman method, Alcian blue -periodic acid Schiff 's (PAS), rapid papanicolaou (PAP) and Gram's stain. (ii) To compare the staining specificity and staining intensity of special stains with respect to routine hematoxylin and eosin (H and E) stain. (iii) To compare the efficacy of special stains to routine H and E stain in identification of the type of keratin present in the selected cases.
A total of 80 cases of known pathology for keratin were retrieved from the department archive, which included 10 each of normal gingiva, hyperkeratosis, squamous papilloma, verrucous hyperplasia, verrucous carcinoma, well-differentiated squamous cell carcinoma, orthokeratinized odontogenic cyst and keratocystic odontogenic tumors. Six sections of 4 µ each from the paraffin blocks were made, stained with H and E and the special stains and these were evaluated by 2 pathologists based on the modified scoring criteria from Rahma Al-Maaini and Philip Bryant 2008.
The results were tabulated using Chi square and kappa statistics. The statistical values for identification of the type of keratinization was insignificant showing that ortho and parakeratinized epithelia could be correctly identified by both H and E as well as all the special stains. Furthermore, all the special stains showed a positive result and statistical significance (P < 0.001) with respect to the staining of keratin.
To conclude, though the special stains distinctly stained the keratin with a higher intensity, H and E proves to be overall better stain with respect to specificity.
角蛋白是最丰富的蛋白质,也是许多上皮病变的典型表现,使其成为组织病理学和免疫组织化学诊断中的重要标志物。由于免疫组织化学是一种昂贵的诊断工具,用于检测角化程度的特殊染色可作为一种更快且经济的选择。本研究的目的是比较角蛋白特殊染色与标准苏木精和伊红染色(H&E)的效果。目标包括:(i)将已诊断的角蛋白疾病病例进行所选特殊染色:阿尤布-施克莱尔法、戴恩-赫尔曼法、阿尔辛蓝-过碘酸希夫氏(PAS)法、快速巴氏(PAP)法和革兰氏染色法。(ii)比较特殊染色相对于常规苏木精和伊红(H&E)染色的染色特异性和染色强度。(iii)比较特殊染色与常规H&E染色在识别所选病例中存在的角蛋白类型方面的效果。
从科室档案中检索出80例已知角蛋白病理的病例,其中包括正常牙龈、角化过度、鳞状乳头瘤、疣状增生、疣状癌、高分化鳞状细胞癌、正角化型牙源性囊肿和角化囊性牙源性肿瘤各10例。从石蜡块中制作6张每张4微米厚的切片,用H&E和特殊染色进行染色,由2名病理学家根据拉赫玛·艾尔-迈尼和菲利普·布莱恩特2008年修改后的评分标准进行评估。
使用卡方检验和kappa统计对结果进行制表。角化类型识别的统计值无显著差异,表明正角化和不全角化上皮均可通过H&E以及所有特殊染色正确识别。此外,所有特殊染色对角蛋白的染色均呈阳性结果且具有统计学意义(P < 0.001)。
总之,尽管特殊染色对角蛋白的染色强度更高,但就特异性而言,H&E被证明是总体上更好的染色方法。