The combination of dermoscopy and reflectance confocal microscopy increases the diagnostic confidence of amelanotic/hypomelanotic lentigo maligna

Author:

Pizzichetta Maria Antonietta12ORCID,Polesel Jerry3,Perrot Jean Luc4,Rubegni Pietro5,Stanganelli Ignazio67,Magi Serena7,Mazzoni Laura7,Farnetani Francesca8ORCID,Pellacani Giovanni9,Garutti Mattia2,Puglisi Fabio210,Cinotti Elisa5,

Affiliation:

1. Department of Dermatology University of Trieste Trieste Italy

2. Department of Medical Oncology Centro di Riferimento Oncologico di Aviano IRCCS, Istituto di ricovero e cura a carattere scientifico Aviano Italy

3. Cancer Epidemiology Unit Centro di Riferimento Oncologico di Aviano IRCCS Aviano Italy

4. Department of Dermatology University Hospital of Saint Etienne Saint‐Etienne France

5. Department of Medical, Surgical and Neurological Science, Dermatology Section University of Siena, S. Maria alle Scotte Hospital Siena Italy

6. Department of Dermatology University of Parma‐Skin Cancer Unit, Istituto Scientifico Romagnolo per lo Studio dei Tumori "Dino Amadori" IRCCS Meldola Italy

7. Skin Cancer Unit IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori" Meldola Italy

8. Department of Dermatology University of Modena and Reggio Emilia Modena Italy

9. Department of Dermatology, Policlinico Umberto I Sapienza University of Rome Rome Italy

10. Department of Medicine University of Udine Udine Italy

Abstract

AbstractThe dermoscopic diagnosis of amelanotic/hypomelanotic lentigo maligna/lentigo maligna melanoma (AHLM/LMM) may be very difficult in its early stages because of lack of pigment. Reflectance confocal microscopy (RCM) is an imaging technique that is especially helpful for the diagnosis of lentigo maligna. To determine the diagnostic performances of dermoscopy and RCM in the diagnosis of AHLM/LMMs we evaluated dermoscopic and RCM images of consecutive cases of histopathologically confirmed AHLM/LMMs, amelanotic/hypomelanotic basal cell carcinoma and squamous cell carcinoma (AHBCCs/AHSCCs), amelanotic/hypomelanotic benign lesions (AHBLs), and actinic keratoses (AKs) from five participating centers. Sensitivity, specificity, accuracy, predictive values, and level of diagnosis confidence were calculated for both diagnostic procedures. Both dermoscopy and RCM showed diagnostic performance >97% in the diagnosis of AHLM/LMMs versus AHBCC/AHSCCs and their combination slightly improved diagnostic performance, with accuracy increasing from 98.0% to 99.1%. Similarly, RCM in combination with dermoscopy showed a tiny increase in the diagnostic performance in the diagnosis of AHLM/LMMs versus AHBLs (accuracy increased from 87.2% to 88.8%) and versus AKs (accuracy increased from 91.4% to 93.4%). Although the increase in diagnostic performance due to RCM was modest, the combination of dermoscopy and RCM greatly increased the level of confidence; high confidence in the diagnosis of AHLM/LMMs versus AHBLs increased from 36.2% with dermoscopy alone to 76.6% with dermoscopy plus RMC. Based on our results, dermoscopy and RCM should be complementary to improve not only diagnostic accuracy but also the level of diagnostic certainty in the diagnosis of AHLM/LMMs.

Publisher

Wiley

Subject

Dermatology,General Medicine

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