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Optical coherence tomography accurately identifies patients with penile (pre) malignant lesions: A single center prospective study.

Ronni Wessels ,
Daniel M De Bruin ,
Dirk J Faber ,
Simon Horenblas ,
Bas W G van Rhijn ,
Andrew D Vincent ,
Marc van Beurden ,
Ton G van Leeuwen ,
Theo J M Ruers

Abstract

MATERIALS AND METHODS

Optical coherence tomography-imaging was performed prior to punch biopsy in 18 consecutive patients with a suspicious lesion at the outpatient clinic of the NKI-AVL. Qualitative analysis consisted of visual assessment of clear layers and a visible lower border of the lesions, quantitative analysis comprised of determination of the epidermal layer thickness and μoct. Results were grouped according to histopathology reports.

CONCLUSION

In this preliminary study, qualitative and quantitative analysis of OCT-images of suspicious penile lesions shows differences between benign lesions and (pre) malignant lesions. These results encourage further research in a larger study population.

RESULTS

Qualitative analysis showed a statistically significant difference (P = 0.047) between benign and (pre) malignant lesions. Quantitative analysis showed that epidermal layer thickness and attenuation coefficient was significantly different between benign and (pre) malignant tissue, respectively, P = 0.001 and P < 0.001.

INTRODUCTION

Currently, (multiple) biopsies are taken to obtain histopathological diagnosis of suspicious lesions of the penile skin. Optical coherence tomography (OCT) provides noninvasive in vivo images from which epidermal layer thickness and attenuation coefficient (μoct) can be quantified. We hypothesize that qualitative (image assessment) and quantitative (epidermal layer thickness and attenuation coefficient, μoct) analysis of penile skin with OCT is possible and may differentiate benign penile tissue from (pre) malignant penile tissue.

More about this publication

Urology annals

Volume 7
Issue nr. 4
Pages 459-65
Publication date 23-12-2015

Full text links

Publisher website (DOI) 10.4103/0974-7796.156147
Europe PubMed Central 26692665
Pubmed 26692665

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