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Table 6 Optical biopsy

From: Current concepts and future of noninvasive procedures for diagnosing oral squamous cell carcinoma - a systematic review

Optical biopsy

Technology

Light source

Information provided

Sensitivity %

Specificity %

Auto-fluorescence spectroscopy

Fluorochromes fluorescence (NAD, FADH)

ultraviolet and visible spectrum light

Distinguish malignant tissue by concentration of (NAD, FADH), re-emit green light

81

100

Enhanced dye fluorescence

Fluorochromes fluorescence (protoporphyrin IX)

ultraviolet and visible spectrum light

Distinguish malignant tissue by high concentration of (protoporphyrin IX), re-emit red light

100

100

Ratio imaging

fluorescence (protoporphyrin IX, NAD, FADH)

ultraviolet and visible blue light

Compare a ratio of red emission of (protoporphyrin IX) from malignant cells with the green emission from normal

from 60 to 97

from 75 to 99%

Raman spectroscopy

Raman vibrational spectroscopy

laser-based spectroscopic technique

enabling chemical characterization

80.5

86.2

Elastic scattering spectroscopy

Elastic scattering (white light reflectance)

pulsed xenon arc lamp

provides optical geometrical information

92

79

Differential path-length spectroscopy

Elastic scattering (white light reflectance)

tungsten-halogen lamp

cell biochemistry, intracellular morphology and microvascular properties such as oxygen saturation and average vessel diameter

69

85

Optical Coherence Tomography

scattered light (Fourier domain mode lock swept source-based) OCT

laser-based

Provide provide high-speed three-dimensional OCT pictures

Subjective image required interpretation

Subjective image required interpretation

Angle-resolved low coherence interferometry (A/LCI)

scattered light to measure the average size of different cell structures

laser-based

delivers direct confirmation of precancerous disease to the physician

100

85