Authors' Affiliations: Laser Microbeam and Medical Program, Beckman Laser Institute, Department of Dermatology, University of California, Irvine, California; JenLab GmbH, Schillerstrasse 1, Jena; and Department of Biophotonics and Laser Technology, Saarland University, Saarbrücken, Germany.
Authors' Affiliations: Laser Microbeam and Medical Program, Beckman Laser Institute, Department of Dermatology, University of California, Irvine, California; JenLab GmbH, Schillerstrasse 1, Jena; and Department of Biophotonics and Laser Technology, Saarland University, Saarbrücken, GermanyAuthors' Affiliations: Laser Microbeam and Medical Program, Beckman Laser Institute, Department of Dermatology, University of California, Irvine, California; JenLab GmbH, Schillerstrasse 1, Jena; and Department of Biophotonics and Laser Technology, Saarland University, Saarbrücken, Germany.
Cancer Res. 2014 May 15;74(10):2688-97. doi: 10.1158/0008-5472.CAN-13-2582. Epub 2014 Mar 31.
Monitoring of atypical nevi is an important step in early detection of melanoma, a clinical imperative in preventing the disease progression. Current standard diagnosis is based on biopsy and histopathologic examination, a method that is invasive and highly dependent upon physician experience. In this work, we used a clinical multiphoton microscope to image in vivo and noninvasively melanocytic nevi at three different stages: common nevi without dysplastic changes, dysplastic nevi with structural and architectural atypia, and melanoma. We analyzed multiphoton microscopy (MPM) images corresponding to 15 lesions (five in each group) both qualitatively and quantitatively. For the qualitative analysis, we identified the morphologic features characteristic of each group. MPM images corresponding to dysplastic nevi and melanoma were compared with standard histopathology to determine correlations between tissue constituents and morphology and to evaluate whether standard histopathology criteria can be identified in the MPM images. Prominent qualitative correlations included the morphology of epidermal keratinocytes, the appearance of nests of nevus cells surrounded by collagen fibers, and the structure of the epidermal-dermal junction. For the quantitative analysis, we defined a numerical multiphoton melanoma index (MMI) based on three-dimensional in vivo image analysis that scores signals derived from two-photon excited fluorescence, second harmonic generation, and melanocyte morphology features on a continuous 9-point scale. Indices corresponding to common nevi (0-1), dysplastic nevi (1-4), and melanoma (5-8) were significantly different (P < 0.05), suggesting the potential of the method to distinguish between melanocytic nevi in vivo.
监测非典型痣是早期发现黑色素瘤的重要步骤,这对于预防疾病进展至关重要。目前的标准诊断基于活检和组织病理学检查,这是一种具有侵入性且高度依赖医生经验的方法。在这项工作中,我们使用临床多光子显微镜对三种不同阶段的黑素细胞痣进行体内非侵入性成像:无发育不良变化的普通痣、具有结构和形态异型性的发育不良痣和黑色素瘤。我们对 15 个病变(每组 5 个)的多光子显微镜 (MPM) 图像进行了定性和定量分析。定性分析中,我们确定了每组特有的形态特征。将发育不良痣和黑色素瘤的 MPM 图像与标准组织病理学进行比较,以确定组织成分与形态之间的相关性,并评估标准组织病理学标准是否可以在 MPM 图像中识别。突出的定性相关性包括表皮角质形成细胞的形态、被胶原纤维包围的痣细胞巢的外观以及表皮-真皮交界处的结构。在定量分析中,我们基于三维体内图像分析定义了一个数值多光子黑色素瘤指数 (MMI),该指数对双光子激发荧光、二次谐波产生和黑素细胞形态特征的信号进行评分,得分范围为连续的 9 分制。普通痣 (0-1)、发育不良痣 (1-4) 和黑色素瘤 (5-8) 的指数差异显著 (P < 0.05),这表明该方法有可能在体内区分黑素细胞痣。