Comparative analysis of dynamic clinical and dermatoscopic characteristics of single and multiple nevi in patients with risk factors for malignant melanoma


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Abstract

Background. Currently, the benefits of dynamic clinical and dermatoscopic follow-up of patients with multiple melanocytic nevi and high risk for melanoma development are widely discussed. Long-term follow-up for patients with a history of melanoma is recommended in a number of international and domestic clinical guidelines for the diagnosis and treatment of this malignant skin tumor. On the other hand, there are practically no data on the management tactics and frequency of observations for patients with single melanocytic nevi, which may have a potential risk of developing malignant melanoma. Objective. Comparison of the frequency of detection of clinical and dermatoscopic changes in single and multiple nevi in patients with a high risk of developing malignant melanoma. Methods. The dynamic follow-up program included 75 patients with one or more risk factors for the development of malignant melanoma, distributed in group I - 43 patients (50 or more melanocytic nevi) and in group II - 32 patients (<50 melanocytic nevi). The patients underwent a questionnaire survey, a clinical dermatological examination, and double photo-mapping with an observation interval of at least 2 months. If significant dermatoscopic changes were detected, an excisional diagnostic biopsy with histological examination was performed. When clinical or dermatoscopic signs suspicious of melanoma were detected, the diagnosis was verified in the settings of an oncological institution. Results. During the follow-up period, out of 9676 studied melanocytic neoplasms in group I, 473 (4.89%) had dynamic dermatoscopic changes, of which 60 (12.7%) were removed with subsequent pathomorphological examination. In group II, 122 (9.58%) of 1274 melanocytic neoplasms changed during dermatoscopic monitoring. Five (4.1%) lesions out of 122 with clinical and dermatoscopic changes were excised for pathomorphological verification of the diagnosis. The proportion of histologically verified melanomas among neoplasms with significant dermatoscopic changes in patients with single nevi was 40%, in patients with multiple nevi - 9.1%. Conclusion. It was found that in patients with single melanocytic nevi and risk factors for the development of melanoma, dynamic changes in dermatoscopic structures in melanocytic nevi were detected no less frequently than in patients with multiple melanocytic nevi (P=0.022). The necessity of including patients with single melanocytic nevi and risk factors in dynamic dermatoscopic follow-up was substantiated.

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About the authors

I. I Vakhitova

Moscow Scientific and Practical Center for Dermatovenereology and Cosmetology

Anna V. Michenko

Medical Research and Education Center, Lomonosov Moscow State University; Central State Medical Academy of Department of Presidential Affairs

Email: amichenko@mail.ru
Cand. Sci. (Med.), Associate Professor at the Department of Dermatovenereology and Cosmetology

K. S Titov

A.S. Loginov Moscow Clinical Scientific Center; RUDN University

A. Yu Brazhnikov

Sechenov University

D. V Romanov

Sechenov University; Research Center for Mental Health

References

  1. Psaty E.L., Scope A., Halpern A.C., et al. Defining the patient at high risk for melanoma. Int J. Dermatol. 2010;49(4):362-76. doi: 10.1111/j.1365-4632.2010.04381.x.
  2. Gandini S., Sera F., Cattaruzza M.S., et al. Meta-analysis of risk factors for cutaneous melanoma: I. Common and atypical naevi. Eur J. Cancer. 2005;41(1):28-44. Doi: 10.1016/j. ejca.2004.10.015.
  3. Kittler H., Marghoob A.A., Argenziano G., et al. Standardization of terminology in dermoscopy/dermatoscopy: results of the third consensus conference of the International Society of Dermoscopy. J. Am Acad Dermatol. 2016;74(6):1093-106. Doi: 10.1016/j. jaad.2015.12.038.
  4. Watts C.G., Dieng M., Morton R.L., et al. Clinical practice guidelines for identification, screening and follow-up of individuals at high risk of primary cutaneous melanoma: a systematic review. Br J. Dermatol. 2015;172(1):33-47. Doi: 10.1111/ bjd.13403.
  5. Salerni G., Carrera C., Lovatto L., et al. Benefits of total body photography and digital dermatoscopy ("two-step method of digital follow-up") in the early diagnosis of melanoma in patients at high risk for melanoma. J. Am Acad Dermatol. 2012;67(1):e17-27. Doi: 10.1016/j. jaad.2011.04.008.
  6. Paul S.P. Micromelanomas: a review of melanomas №2 mm and a case report. Case Rep Oncol Med. 2014;2014:206260. doi: 10.1155/2014/206260.
  7. Inskip M., Magee J., Weedon D., et al. When algorithms falter: a case report of a very small melanoma excised due to the dermatoscopic «ugly duckling» sign. Dermatol. Pract Concept. 2013;3(2):59-62. doi: 10.5826/dpc.0302a09.
  8. Geller A.C., Mayer J.E., Sober A.J., et al. Total nevi, atypical nevi and melanoma thickness an anakysis of 566 patients at 2 US centers. JAMA. Dermatol. 2016;152(4):413-18. Doi: 10.1001/ jamadermatol.2016.0027.
  9. Cust A.E., Goumas C., Holland E.A., et al. MC1R genotypes and risk of melanoma before age 40 years: a population-based case-control-family study. Int J. Cancer 2012;131:E269-81. doi: 10.1002/ijc.27357.
  10. Menzies S.W., Gutenev A., Avramidis M., et al. Short-term digital surface microscopic monitoring of atypical or changing melanocytic lesions. Arch Dermatol. 2001;137(12):1583-89. doi: 10.1001/archderm.137.12.1583.
  11. Kittler H., Pehamberger H., Wolff K., et al. Follow-up of melanocytic skin lesions with digital epiluminescence microscopy: patterns of modifications observed in early melanoma, atypical nevi, and common nevi. J. Am Acad Dermatol. 2000;43(3):467-76. Doi: 10.1067/ mjd.2000.107504.
  12. Schiffner R., Schiffner-Rohe J., Landthaler M., et al. Long-term dermoscopic follow-up of melanocytic naevi: clinical outcome and patient compliance. Br J. Dermatol. 2003;149(1):79-86. doi: 10.1046/j.1365-2133.2003.05409.x.
  13. Fikrle T., Pizinger K., Szakos H., et al. Digital dermatoscopic follow-up of 1027 melanocytic lesions in 121 patients at risk of malignant melanoma. J. Eur Acad Dermatol Venereol. 2013;27(2):180-86. doi: 10.1111/j.1468- 3083.2011.04438.x.
  14. Rotaru M., Nati A.E., Avramoiu I., et al. Digital dermoscopic follow-up of 1544 melanocytic nevi. Rom J. Morphol Embryol. 2015;56(4):1467-72.
  15. Argenziano G., Giacomel J., Zalaudek I., et al. A clinico-dermoscopic approach for skin cancer screening: recommendations involving a survey of the International Dermoscopy Society. Giuseppe Argenziano et al. Dermatol Clin. 2013;31(4):525 34, vii. doi: 10.1016/j.det.2013.06.001
  16. O'Neill C.H., Scoggins C.R. Melanoma. J Surg Oncol. 2019;120(5):873-81. Doi: 10.1002/ jso.25604
  17. Buhl T., Hansen-Hagge C, Korpas B., et al. Integrating static and dynamic features of melanoma: The DynaMel algorithm. J Am Acad Dermatol. 2012.66:27-36. Doi: 10.1016/j. jaad.2010.09.731

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