This article is part of the supplement: 1st Scientific Meeting of the Head and Neck Optical Diagnostics Society
Oral presentation
Interrogation of skin pathology using elastic scattering spectroscopy
Head & Neck Oncology 2009, 1(Suppl 1):O19 doi:10.1186/1758-3284-1-S1-O19
The electronic version of this article is the complete one and can be found online at: http://www.headandneckoncology.org/content/1/S1/O19
| Published: | 28 July 2009 |
© 2009 Jiao et al; licensee BioMed Central Ltd.
Introduction
Optical biopsies have been shown to be very effective in providing real time, in situ and non-invasive diagnosis of various tissue pathologies. In the head and neck various tissues have been interrogated using this modality including suspicious oral lesions, tumour resection margins and metastatic lymph nodes.
Elastic scattering spectroscopy (ESS) is one of the optical modalities used to identify inflammatory, ischaemic, premalignant and malignant malformation through changes on the cellular and subcellular level.
The aim of this study was to see if ESS could be used to identify benign and malignant skin lesions.
Materials and methods
Elastic scattering spectroscopy involves firing a xenon-arc lamp light into tissues using a fibre-optic probe. Light undergoes single or multiple scattering events and is then collected by the same probe. The resultant generated spectra are then compared to gold standard histopathology.
In this study, facial skin lesions acquired from 73 patients were subjected to in vivo elastic scattering spectroscopy. Lesions were then surgically resected. The majority of the lesions were classified into four categories: basal cell carcinoma, seborrhic keratosis, fibroepithelial polyp and intradermal nevi.
Results
Results showed that ESS can differentiate between normal and pathological skin conditions as well as benign and malignant skin conditions.
Conclusion
This technology holds great promise. A larger body of data is required to achieve higher sensitivity and specificity. Future data will be acquired from malignant melanoma lesions to enable comparison with benign pigmented skin conditions.