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Cancer Res. 2014 May 15;74(10):2688-97. doi: 10.1158/0008-5472.CAN-13-2582. Epub 2014 Mar 31.

Distinguishing between benign and malignant melanocytic nevi by in vivo multiphoton microscopy.

Author information

1
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.
2
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.
3
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 bjtrombe@uci.edu.

Abstract

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.

PMID:
24686168
PMCID:
PMC4024350
DOI:
10.1158/0008-5472.CAN-13-2582
[Indexed for MEDLINE]
Free PMC Article

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