首页> 外文期刊>American Journal of Dermatopathology >A Comparative Study of Immunohistochemical Myoepithelial Cell Markers in Cutaneous Benign Cystic Apocrine Lesions
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A Comparative Study of Immunohistochemical Myoepithelial Cell Markers in Cutaneous Benign Cystic Apocrine Lesions

机译:免疫组织化学肌上皮细胞标志物在皮肤良态囊性阴影病变中的比较研究

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The use of immunohistochemical markers for myoepithelial cells (MEC) is a useful tool in the distinction of benign from malignant epithelial neoplasms. Although their use in breast tumors is well recognized, little is known concerning its application in comparable cutaneous lesions. Using benign cutaneous cystic apocrine lesions as a study model, the aim of this study was to compare 5 immunohistochemical markers [calponin, p63, smooth muscle actin (SMA), cytokeratin 14, and CD10] in their effectiveness to highlight MEC. Cases of apocrine hidrocystoma and cystadenoma (n = 44) were reviewed with a particular emphasis on proliferative features and apocrine change. The MEC staining pattern and the intensity and distribution scores in proliferative (n = 29) and nonproliferative (n = 15) lesions were assessed, and the differences between the 2 groups were statistically analyzed using Fisher exact test. Calponin and SMA stained MEC in the most consistent manner. Being a nuclear stain, p63 was easy to interpret but typically showed discontinuous staining. Cytokeratin 14 not only effectively highlighted MEC but also stained some luminal epithelial cells in an unpredictable manner. Because of prominent background dermal fibroblast staining, CD10 was often difficult to interpret. Only SMA and p63 showed a statistically significant difference in MEC staining intensity scores between the proliferative and nonproliferative groups. Our results show that immunohistological staining for MEC in benign cystic apocrine lesions of the skin is variable. The authors recommend that a panel of markers that includes calponin and p63 be used and highlight the need for awareness of specific caveats associated with individual markers.
机译:用于肌上皮细胞(MEC)的免疫组织化学标志物是一种有用的恶性上皮肿瘤区别良性的工具。虽然它们在乳腺肿瘤中的使用很好地认识到,但众所周知的是其在可比皮肤病变中的应用。使用良性皮肤囊性口腔病变作为研究模式,本研究的目的是将5个免疫组织化学标记[Calponin,P63,平滑肌肌动蛋白(SMA),细胞核酸汀14和CD10]以其有效地进行比较,以突出MEC。通过特别强调增殖特征和口腔变化,综述了血清杂菌瘤和胱前瘤(n = 44)的病例。评估MEC染色图案和增殖(n = 29)和非增殖(n = 15)病变中的强度和分布评分,并且使用Fisher精确测试统计分析2组之间的差异。 Calponin和SMA以最常见的方式染色了MEC。核污渍,P63易于解释,但通常显示出不连续的染色。细胞角蛋白14不仅有效地突出显示MEC,还以不可预测的方式染色一些腔上皮细胞。由于突出的背景皮肤成纤维细胞染色,CD10通常难以解释。只有SMA和P63才显示出增殖和不增殖组之间的MEC染色强度分数统计学差异。我们的结果表明,皮肤良性囊性口腔病变中MEC的免疫组织染色是可变的。作者建议使用包括Calponin和P63的标记面板,并突出需要了解与个别标记相关的特定警告的认识。

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