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首页> 外文期刊>Melanoma research >Quantitative measurements of formalin-induced fluorescence for differential diagnostics of melanomas and lesions of human skin.
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Quantitative measurements of formalin-induced fluorescence for differential diagnostics of melanomas and lesions of human skin.

机译:福尔马林诱导的荧光的定量测量,用于对人皮肤黑色素瘤和病变进行鉴别诊断。

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The usefulness of formaldehyde-induced fluorescence (FIF) for detection of melanoma cells has been suggested by several investigators during the last 40 years. FIF can be easily excited and observed in microscopic sections of formalin-fixed paraffin-embedded skin samples. However, such an approach has never been widely used in melanoma diagnostics for reasons including lack of clear diagnostic criteria, considerable inconsistencies in both the protocols used and qualitatively analysed results reported by different groups. This study aimed at determination of the spectral bands optimum for detecting melanoma cells. The study involved three sets of the excitation and emission bands: gammaex=366 nm, gammaem>425 nm; gammaex=450-480 nm, gammaem>515 nm; gammaex=450-480 nm, gammaem=510-550 nm. Microscopic digital imaging was used to quantitatively determine the fluorescence intensity of 53 primary melanomas and 32 benign lesions. Best classification of melanomas with algorithm based on fluorescence intensity threshold was obtained for gammaex=450-480 nm, gammaem=510-550 nm. Receiver operating characteristics (ROC) analysis of the algorithm yielded area under the curve=0.84 +/- 0.05 for melanocytic cells present in the stratum corneum. Our results clearly indicate that the FIF emitting molecules (most probably 5-S-cysteinyldopa) are present in melanomas at the concentration significantly higher than in benign lesions. In terms of the ROC analysis, the diagnostic performance of the test based on the FIF intensity is as good as of many other commonly used diagnostic tests.
机译:在过去的40年中,一些研究人员提出了甲醛诱导的荧光(FIF)检测黑色素瘤细胞的有用性。在福尔马林固定石蜡包埋的皮肤样品的显微切片中,可以很容易地激发并观察到FIF。但是,由于缺乏明确的诊断标准,所使用的方案中存在明显的不一致以及不同小组报告的定性分析结果等原因,这种方法从未在黑素瘤诊断中广泛使用。这项研究旨在确定最适合检测黑素瘤细胞的光谱带。该研究涉及三组激发和发射带:γ= 366 nm,γ> 425 nm;以及gammaex = 450-480 nm,gammaem> 515 nm; gammaex = 450-480 nm,gammaem = 510-550 nm。显微数字成像用于定量确定53例原发性黑色素瘤和32例良性病变的荧光强度。对于gammaex = 450-480 nm,gammaem = 510-550 nm,使用基于荧光强度阈值的算法对黑素瘤进行了最佳分类。该算法的接收器工作特征(ROC)分析得出了角质层中存在的黑素细胞的曲线下面积= 0.84 +/- 0.05。我们的结果清楚地表明,黑色素瘤中存在的FIF发射分子(最可能是5-S-半胱氨酰多巴)的浓度明显高于良性病变。在ROC分析方面,基于FIF强度的测试的诊断性能与许多其他常用的诊断测试一样好。

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