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使用视频图像分析测量黑素细胞肿瘤中的S100蛋白和神经元特异性烯醇化酶

Measuring S100 protein and neurone specific enolase in melanocytic tumours using video image analysis.

作者信息

Williams R A, Rode J, Dhillon A P, Jarvis L R, Skinner J M, Jamal O

出版信息

J Clin Pathol. 1986 Oct;39(10):1096-8. doi: 10.1136/jcp.39.10.1096.

Abstract

Using a computed video image analysis system, the staining intensity for both neurone specific enolase (NSE) and S100 protein was measured in sections from 19 malignant melanomas and 16 benign melanocytic lesions. The results of this study confirm previous reports that NSE and S100 protein are useful markers for malignant melanoma. NSE staining intensity in the cases of malignant melanoma was significantly higher than that in benign naevi (p = 0.011). Intensity of staining for S100 protein was not significantly higher in the malignant melanomas. There was, however, a significant S100 gradient when comparing superficial and deep intradermal portions of these tumours (p = 0.003). This feature was not seen in benign naevi. The greatest intensity of S100 protein staining was found in the deeper portions of the malignant melanomas. This gradient difference was not seen with staining for NSE. Although it seems that the overall intensity of staining for NSE is more effective in differentiating between benign and malignant lesions, the difference in staining intensity between the superficial and deep portions of the tumour may be the better indicator of adverse behaviour in lesions in which the diagnosis of malignancy is uncertain.

摘要

使用计算机视频图像分析系统,对19例恶性黑色素瘤和16例良性黑素细胞病变的切片中神经元特异性烯醇化酶(NSE)和S100蛋白的染色强度进行了测量。本研究结果证实了先前的报道,即NSE和S100蛋白是恶性黑色素瘤的有用标志物。恶性黑色素瘤病例中的NSE染色强度显著高于良性痣(p = 0.011)。恶性黑色素瘤中S100蛋白的染色强度没有显著更高。然而,在比较这些肿瘤的真皮浅层和深层部分时,存在显著的S100梯度(p = 0.003)。在良性痣中未观察到这一特征。S100蛋白染色强度最高的部位是恶性黑色素瘤的较深部分。NSE染色未观察到这种梯度差异。虽然似乎NSE染色的总体强度在区分良性和恶性病变方面更有效,但肿瘤浅层和深层之间染色强度的差异可能是在恶性诊断不确定的病变中提示不良行为的更好指标。

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