Clinical and Dermoscopic Features of Lentigo Maligna

  • prof. dr Danica Tiodorovic prof. dr Danica Tiodorovic
  • Daanijela Popović
  • Slađana Cekić
  • Milica Radić
  • Aleksandar Popović
  • Nataša Vidović
  • Andrija Jović

Abstract


This study aimed analyze the clinical and dermoscopic features of patients with pathohistologically verified lentigo maligna (LM) and to determine possible influence of anatomical topography, age and gender in the dermoscopic features of LM.

Our retrospective study included 32 patients with 32 LMs in total, diagnosed between 2017 and 2020. Clinical data recorded from each patient included the following: demographic features (age, gender), anatomic localization (facial or extrafacial) and clinical size (<10mm or >10 mm). Facial area was subdivided into 8 topographical sites, while extrafacial localization involved any location outside the face region. All dermoscopic images were analyzed for the presence of dermoscopic features previously described for LM.

In the total of 32 patients, there were 19 males and 13 females. The patients age ranged from 34 to 80 years (median age 60.1±10.4 years).  Significant female predominance was observed for localization on the cheeks (p=0.018). Localization on the nose was significantly associated with patients older than 65 (p=0.039). The most frequent dermoscopic features were asymmetric pigmented follicular openings 23 (71.9%), gray color 22 (68.8%) and pigmented rhomboidal structures 15 (46.9%). In relation to age and specific dermoscopic features, gray color (p=0.035) and white scar-like areas were (p=0.012) significantly higher in patients older than 65, while pigmented rhomboidal structures (p=0.041) were significantly associated with younger patients.

The observed differences in the frequency of clinical and dermoscopic features of LM have significant importance in everyday clinical practice and can assist clinicians in the early diagnosis of this malignant tumor

References


1. Clark WH Jr, Mihm MC Jr. Lentigo maligna and lentigo-maligna melanoma. Am J Pathol. 1969;55(1):39-67.


2. Hutchinson J. Senile freckles. Arch. Surg. 1882; 3: 319–22.


3. Becker SW. Dermatological investigations of melanin pigmentation. In: Braaten D (ed.). The Biology of Melanoma, Vol. IV. New York, NY: Special Publications of the New York Academy of Sciences, 1948; 82–125.


4. Flotte TJ, Mihm MC Jr. Lentigo maligna and malignant melanomain situ, lentigo maligna type. Hum. Pathol. 1999; 30: 533–6.


5. Tannous ZA, Lerner LH, Duncan LM et al. Progression to invasive melanoma from malignant melanoma in situ, lentigo maligna type. Hum. Pathol. 2000; 31: 705–8.


6. Higgins HW 2nd, Lee KC, Galan A, Leffell DJ. Melanoma in situ: Part I. Epidemiology, screening, and clinical features. J Am Acad Dermatol. 2015;73(2):181-90.


7. Swetter SM, Boldrick JC, Jung SY, et al. Increasing incidence of lentigo maligna melanoma subtypes: northern California and national trends 1990-2000. J Invest Dermatol. 2005;125(4):685-91.


8. Durnick A, Stolz W, Landthaler M et al. Lentigo maligna and lentigo maligna melanoma in young adults. Dermatol. Surg. 2004; 30: 813–64.


9. Smalberger GJ, Siegel DM, Khachemoune A. Lentigo maligna. Dermatol Ther. 2008;21(6):439-46.


10. Schiffner R, Schiffner-Rohe J, Vogt T, et al. Improvement of early recognition of lentigo maligna using dermatoscopy. J Am Acad Dermatol. 2000;42(1 Pt 1):25 32


11.  Pralong P, Bathelier E, Dalle S, et al.Dermoscopy of lentigo maligna melanoma: report of 125 cases. Br J Dermatol. 2012 Aug;167(2):280-7.


12. Tiodorovic-Zivkovic D, Zalaudek I, Lallas A, et al. The importance of gray color as a dermoscopic clue in facial pigmented lesion evaluation: a case report. Dermatol Pract Concept. 2013;3(4):37-9.


13. Peris, K., Maiorino, A., Di Stefani, et al. Brown globules in lentigo maligna (LM): a useful dermoscopic clue. J Am Acad Dermatol. 2016; 75(2), 429-430.


14. Tiodorovic-Zivkovic D, Argenziano G, Lallas A, et al. Age,gender, and topography influence the clinical and dermoscopic appearance of lentigo maligna. J Am Acad Dermatol. 2015;72(5):801-8.


15. Guitera P, Collgros H, Madronio CM, et al. The steadily growing problem of lentigo maligna and lentigo maligna melanoma in Australia: Population-based data on diagnosis and management. Australas J Dermatol. 2019;60(2):118-125.


16. Aitken JF, Youlden DR, Baade PD et al. Generational shift in melanoma incidence and mortality in Queensland, Australia, 1995–2014. Int. J. Cancer 2018; 142: 1528–35.


17. Matas-Nadal C, Malvehy J, Ferreres JR, et al. Increasing incidence of lentigo maligna and lentigo maligna melanoma in Catalonia. Int J Dermatol. 2019 May;58(5):577-581.


18. Higgins HW 2nd, Cho E, Weinstock MA et al. Gender differences, UV exposure and risk of lentigo maligna in a nationwide healthcare population cohort study. J Eur Acad Dermatol Venereol. 2019;33(7):1268-1271.


19. Lallas A, Tschandl P, Kyrgidis A, et al. Dermoscopic clues to differentiate facial lentigo maligna from pigmented actinic keratosis. Br J Dermatol. 2016 ;174(5):1079-85

Published
2025/12/19
Section
Originalni rad / Original article