Volume 93, Issue S255
ABS15-0591
Free Access

New management of peri-ocular basal cell carcinoma using in vivo and ex vivo confocal microscopes

M. Espinasse

M. Espinasse

Laboratory Biology- Engineering and Imaging of Corneal Graft- EA2521, University Jean Monnet- Faculty of Medicine, Saint-Etienne, France

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D. Grivet

D. Grivet

Ophthalmology, University Hospital, Saint-Etienne, France

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J.L. Perrot

J.L. Perrot

Dermatology, University Hospital, Saint-Etienne, France

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E. Cinotti

E. Cinotti

Dermatology, University Hospital, Saint-Etienne, France

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B. Labeille

B. Labeille

Dermatology, University Hospital, Saint-Etienne, France

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F. Forest

F. Forest

Pathology, Hospital University, Saint-Etienne, France

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P. Gain

P. Gain

Ophtalmology, University Hospital, Saint-Etienne, France

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G. Thuret

G. Thuret

Corneal Graft Biology- Engineering and Imaging Laboratory- EA2521- Federative Institute of Research in Sciences and Health Engineering- Faculty of Medicine and Institut Universitaire de France- Bd St Michel- Paris- France, University Jean Monnet, Saint-Etienne, France

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First published: 23 September 2015

Abstract

Purpose

We have been using a handheld dermatology in vivo reflectance confocal microscopy (IVCM) for the imaging of the whole ocular surface and ocular adnexa for more than two year (JAmAcadDermatol2014;71:912, AJO2015;159:324), mainly for noninvasive diagnosis before surgery. Ex vivo confocal microscopy (EVCM) is a new device that allows pseudo histology in freshly excised tissue. Aim: to assess a new management strategy for eyelids lesions suspected to be basal cell carcinoma (BCC) using these two complementary confocal microscopes (CM).

Methods

IVCM and EVCM, both using vivascope CM (Lucid Inc, NY) were performed by 3 skilled dermatologists having more than 500 CM diagnoses each with pathology confirmation. Forty consecutive peri-ocular BCC were diagnosed by IVCM. Two millimetre-margin incisions were made during surgery. Freshly excised tissues were mounted, unstained, between two glass slides and analysed “en face” with EVCM to delimitated the tumour and the clearance of margins. Diagnosis and margins were confirmed by standard pathology and immunolabeling on fixed tissues.

Results

We obtained the first “en face” EVCM to delimitated the tumour. The acquisition of the whole tumour took less than 3 minutes. Tissues were not damaged by flat mount nor by exposure to laser beam. Histology confirmed all IVCM diagnosis of BCC and all clear margins.

Conclusions

Association of IVCM and EVCM allowed accurate management of peri ocular BCC, using micrographic surgery to reduced surgical margins. GRANT: project INNOVEYE GIRCI RAA.

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