Paper
10 February 2007 Time-resolved multiphoton imaging of basal cell carcinoma
R. Cicchi, S. Sestini, V. De Giorgi, D. Stambouli, P. Carli, D. Massi, F. S. Pavone
Author Affiliations +
Abstract
We investigated human cutaneous basal cell carcinoma ex-vivo samples by combined time resolved two photon intrinsic fluorescence and second harmonic generation microscopy. Morphological and spectroscopic differences were found between malignant skin and corresponding healthy skin tissues. In comparison with normal healthy skin, cancer tissue showed a different morphology and a mean fluorescence lifetime distribution slightly shifted towards higher values. Topical application of delta-aminolevulinic acid to the lesion four hours before excision resulted in an enhancement of the fluorescence signal arising from malignant tissue, due to the accumulation of protoporphyrines inside tumor cells. Contrast enhancement was prevalent at tumor borders by both two photon fluorescence microscopy and fluorescence lifetime imaging. Fluorescence-based images showed a good correlation with conventional histopathological analysis, thereby supporting the diagnostic accuracy of this novel method. Combined morphological and lifetime analysis in the study of ex-vivo skin samples discriminated benign from malignant tissues, thus offering a reliable, non-invasive tool for the in-vivo analysis of inflammatory and neoplastic skin lesions.
© (2007) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
R. Cicchi, S. Sestini, V. De Giorgi, D. Stambouli, P. Carli, D. Massi, and F. S. Pavone "Time-resolved multiphoton imaging of basal cell carcinoma", Proc. SPIE 6442, Multiphoton Microscopy in the Biomedical Sciences VII, 64421I (10 February 2007); https://doi.org/10.1117/12.700216
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Cited by 2 scholarly publications.
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KEYWORDS
Skin

Tissues

Luminescence

Microscopy

Second-harmonic generation

Fluorescence lifetime imaging

Tissue optics

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