Non-invasive in vivo dermatopathology: identification of reflectance confocal microscopic correlates to specific histological features seen in melanocytic neoplasms
Article first published online: 23 OCT 2013
© 2013 European Academy of Dermatology and Venereology
Journal of the European Academy of Dermatology and Venereology
Volume 28, Issue 8, pages 1069–1078, August 2014
How to Cite
Gill, M., Longo, C., Farnetani, F., Cesinaro, A.M., González, S. and Pellacani, G. (2014), Non-invasive in vivo dermatopathology: identification of reflectance confocal microscopic correlates to specific histological features seen in melanocytic neoplasms. Journal of the European Academy of Dermatology and Venereology, 28: 1069–1078. doi: 10.1111/jdv.12285
- Conflicts of interest
- Conflicts of interest
- Dr M. Gill and Dr S. González were previously investigators for an NCI-funded study granted to Lucid Inc., original manufacter of the device for this study. Dr S. González serves as consultant for Lucid. Inc. Dr M. Gill was paid a nominal fee directly from the study funds to participate as one of several investigators. G. Pellacani received honoraria for courses and acted as consult for MAVIG gmbh and Caliber ID.
- Funding sources
- This study is supported by the Grant of the Istituto Superiore di Sanità (ISS), Italy (project nr. 527/B/3A/4).
- Issue published online: 8 AUG 2014
- Article first published online: 23 OCT 2013
- Manuscript Accepted: 16 SEP 2013
- Manuscript Received: 7 JUN 2013
- Istituto Superiore di Sanità (ISS). Grant Number: 527/B/3A/4
Reflectance confocal microscopy (RCM) allows for non-invasive, in vivo evaluation of skin lesions and it has been extensively applied in skin oncology although systematic studies on nevi characterization are still lacking.
The aim of this study was to determine whether reliable RCM correlates to histological features used to diagnose melanocytic neoplasms exist.
We blindly evaluated the RCM and histological features of 64 melanocytic neoplasms (19 non-dysplastic nevi, 27 dysplastic nevi, 14 melanomas) and analysed the data using Spearman's rho calculation.
Many histological features can be identified using RCM. Elongated rete ridges corresponded on RCM to edge papillae, whereas flattened rete ridges to several features which involve dermal–epidermal junction disruption. Bridging of junctional nesting (JN) corresponded on RCM to both JN with irregular size/shape and JN with short interconnections. While we could reliably identify dermal melanocytes, the RCM features did not reliably distinguish between benign and concerning dermal melanocytic arrangements, suggesting further refinement of dermal melanocytic RCM features is needed.
Reliable correlates for epidermal and junctional histological features used to diagnose melanocytic neoplasms are identifiable on RCM, suggesting harnessing histological criteria may be a reasonable method to move beyond the algorithmic approach.