M. Rajadhyaksha et al., IN-VIVO CONFOCAL SCANNING LASER MICROSCOPY OF HUMAN SKIN - MELANIN PROVIDES STRONG CONTRAST, Journal of investigative dermatology, 104(6), 1995, pp. 946-952
Confocal scanning laser microscopy of live human skin was performed to
investigate the correlation of in vivo cellular and morphologic featu
res to histology, the effect of wavelength on imaging, and the role of
melanin as a contrast agent. We built a video-rate confocal scanning
laser microscope for in vivo imaging of human skin. Using a 100 x micr
oscope objective, we imaged high-contrast optical ''sections'' of norm
al skin, vitiliginous skin, and a compound nevus. In vivo ''confocal h
istology'' correlated well with conventional histology. The maximum im
aging depth increased with wavelength: the epidermis was imaged with v
isible 400-700-nm wavelengths; the superficial papillary dermis and bl
ood cells (erythrocytes and leukocytes) in the deeper capillaries were
imaged with the near infrared 800-900-nm wavelengths. For confocal re
flectance imaging, melanin provided strong contrast by increased backs
cattering of light such that the cytoplasm in heavily pigmented cells
imaged brightly. In vivo confocal microscopy potentially offers dermat
ologists a diagnostic tool that is instant and entirely non-invasive c
ompared to conventional histopathology.