Lentigo maligna: a review

Author:

Karponis Dimitrios1ORCID,Stratigos Ioannis A2,Joshy Jilse12,Craig Paul J3,Mistry Khaylen1ORCID,van Bodegraven Birgitta45,Venables Zoe C126,Levell Nick J12ORCID

Affiliation:

1. Department of Dermatology, Norfolk and Norwich University Hospital , Norwich , UK

2. Norwich Medical School, University of East Anglia , Norwich , UK

3. Cellular Pathology, Gloucestershire Hospitals NHS Foundation Trust , Cheltenham , UK

4. British Association of Dermatologists , London , UK

5. National Disease Registration Service , Data and Analytics, NHS England , UK

6. National Disease Registration Service , Data and Analytics , NHS England, UK

Abstract

Abstract Lentigo maligna (LM) is a melanoma in situ with distinct clinical features and histology. It commonly affects men after the sixth decade of life. Incidence rates of LM have increased based on early 21st century data from different countries; however, data are suboptimal. Data from England show a plateauing crude incidence between 2013 and 2019. By comparison, invasive melanoma and other types of melanoma in situ commonly appears in younger age groups (median age 58 and 67 years old, respectively) and incidence is rising. The most important risk factors for LM include fair skin and cumulative ultraviolet solar radiation exposure. Although LM is limited to the epidermis and connected skin adnexa, it may progress to invasive LM melanoma. The reported rate of malignant progression varies, reflecting a challenge for LM epidemiology research as often lesions are removed on diagnosis. LM poses a challenge in diagnosis and management. Although it can be diagnosed clinically or dermoscopically, histopathological assessment of biopsied skin tissue remains the gold standard. Reflectance confocal microscopy allows for better appreciation of the complexity of LM at a cellular level, often progressing beyond clinical margins. Management of LM may involve Mohs micrographic surgery or excision, although recurrence may occur even with 5 mm clinical margins. Imiquimod cream may be effective, but incomplete treatment and recurrence has been reported. Conservative management with observation or radiotherapy may be used in selected patients’ cases. Five-year net survival rates are excellent. This paper reviews the natural history, epidemiology, aetiology, pathogenesis, diagnosis and management of LM.

Publisher

Oxford University Press (OUP)

Subject

Dermatology

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