Histological correlates of optical coherence tomography in non-melanoma skin cancer

Background Non‐melanoma skin cancer (NMSC) is rarely fatal but is now the most common malignancy occurring in white populations, accounting for 70% of the cost of managing skin cancer. Optical coherence tomography (OCT) has the potential to improve diagnostic accuracy and help delineate pre‐surgical...

Full description

Saved in:
Bibliographic Details
Published inSkin research and technology Vol. 19; no. 1; pp. e10 - e19
Main Authors Coleman, Andrew John, Richardson, Thomas James, Orchard, Guy, Uddin, Ayesha, Choi, Min Joo, Lacy, Katie Elizabeth
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.02.2013
John Wiley & Sons, Inc
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Background Non‐melanoma skin cancer (NMSC) is rarely fatal but is now the most common malignancy occurring in white populations, accounting for 70% of the cost of managing skin cancer. Optical coherence tomography (OCT) has the potential to improve diagnostic accuracy and help delineate pre‐surgical margins in NMSC. Its widespread clinical acceptance awaits the accumulation of evidence from studies of direct histological comparisons. Method In this study, seventy‐eight subjects presenting with skin lesions, including 28 NMSCs, were imaged using the VivoSight® OCT scanner and a biopsy taken. Haemotoxylin and eosin stained histology sections were compared with the OCT images. Results The depth of superficial basal cell carcinoma (BCC) lesions (<1 mm) can be measured accurately using OCT. A low‐strength OCT signal at the periphery of the cell nests seen in superficial and nodular BCC is identified as corresponding to cellular palisading. A weak inverse linear correlation (r2 = 0.3) is found between the optical attenuation coefficient measured on OCT and the nuclear‐cytoplasmic ratio (N/C) of cells determined from histology. Conclusions OCT has clinical value in providing accurate dimensional measurement of superficial BCC and in identifying the presence of peripheral palisading in nodular BCC.
Bibliography:ark:/67375/WNG-5KW7467K-H
istex:8D46C81A620344BB86DD2C9C7FBAA36A499C1FDE
ArticleID:SRT626
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 14
content type line 23
ISSN:0909-752X
1600-0846
1600-0846
DOI:10.1111/j.1600-0846.2012.00626.x