首页 | 本学科首页   官方微博 | 高级检索  
     


In vivo study for the discrimination of cancerous and normal skin using fibre probe‐based Raman spectroscopy
Authors:Carina Reble  Ingo Gersonde  Jürgen Helfmann  Joachim W. Fluhr  Jürgen Lademann  Joachim Röwert‐Huber  Alexa Patzelt  Martina C. Meinke
Affiliation:1. Laser‐ und Medizin‐Technologie Berlin (LMTB), Berlin, Germany;2. Institut für Optik und Atomare Physik, Technische Universit?t Berlin, Berlin, Germany;3. Department of Dermatology, Venerology and Allergology, Charité – Universit?tsmedizin Berlin, Berlin, Germany
Abstract:Raman spectroscopy has proved its capability as an objective, non‐invasive tool for the detection of various melanoma and non‐melanoma skin cancers (NMSC) in a number of studies. Most publications are based on a Raman microspectroscopic ex vivo approach. In this in vivo clinical evaluation, we apply Raman spectroscopy using a fibre‐coupled probe that allows access to a multitude of affected body sites. The probe design is optimized for epithelial sensitivity, whereby a large part of the detected signal originates from within the epidermal layer's depth down to the basal membrane where early stages of skin cancer develop. Data analysis was performed on measurements of 104 subjects scheduled for excision of lesions suspected of being malignant melanoma (MM) (n = 36), basal cell carcinoma (BCC) (n = 39) and squamous cell carcinoma (SCC) (n = 29). NMSC were discriminated from normal skin with a balanced accuracy of 73% (BCC) and 85% (SCC) using partial least squares discriminant analysis (PLS‐DA). Discriminating MM and pigmented nevi (PN) resulted in a balanced accuracy of 91%. These results lie within the range of comparable in vivo studies and the accuracies achieved by trained dermatologists using dermoscopy. Discrimination proved to be unsuccessful between cancerous lesions and suspicious lesions that had been histopathologically verified as benign by dermoscopy.
Keywords:fibre probe     in   vivo     optical diagnosis  Raman spectroscopy  skin cancer
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号