A novel imaging approach to periocular basal cell carcinoma: In vivo optical coherence tomography and histological correlates

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Abstract

PurposeOptical coherence tomography (OCT) is a non-invasive imaging method widely used in ophthalmology. Recent developments have produced OCT devices for imaging the skin. The purpose of this study was to investigate Fourier Domain OCT morphological features of periocular basal cell carcinoma (BCC) in correlation with conventional histopathology.MethodsConsecutive patients with periocular nodular BCC were prospectively examined with VivoSight OCT (Michelson Ltd) prior to surgical excision. OCT slice mode images were analysed using criteria defined for conventional and HD-OCT; the images were correlated to haematoxylin and eosin stained histology sections.ResultsA total of 15 patients with periocular BCC were recruited. Three categories of BCC morphological features were identified from slice mode OCT images: 1) Epidermal changes included epidermal thinning (15/15; 100%), ulceration and crusting (5/15, 33.3%) and decreased density of hair follicles (8/15; 53.3%); 2) Intralesional features included hyporeflective nodules (15/15; 100%), hyper-reflective edges (15/15; 100%) and hyporeflective central necrosis (3/15; 20%) 3) Perilesional features included hyporeflective borders (11/15; 73%), hypereflective margins (15/15; 100%) and dilated blood vessels (5/15; 33%).ConclusionsThis study demonstrated that Fourier Domain OCT imaging offers additional information in the identification of morphological features of nodular BCC compared to conventional OCT diagnostic criteria. VivoSight produced fast, non-invasive imaging of skin lesions in the periocular region and high correlation with histology. Further studies are necessary to investigate OCT features of different histological subtypes of BCC.

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Pelosini, L., Smith, H. B., Schofield, J. B., Meeckings, A., Dithal, A., & Khandwala, M. (2015). A novel imaging approach to periocular basal cell carcinoma: In vivo optical coherence tomography and histological correlates. Eye (Basingstoke), 29(8), 1092–1098. https://doi.org/10.1038/eye.2015.97

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