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Pigmented Naevi and Their Relationship to Malignant Melanoma


Authors: S. Pavel;  K. Pizinger
Authors place of work: přednosta prof. MUDr. Karel Pizinger, CSc. ;  Dermatolovenerologická klinika LF UK a FN Plzeň
Published in the journal: Čes-slov Derm, 86, 2011, No. 6, p. 263-271
Category: Reviews (Continuing Medical Education)

Summary

The development of a higher number of pigmented naevi is an important risk factor for melanoma. This is especially true for larger, so-called clinically atypical or dysplastic naevi. These naevi develop more frequently in people with a fair skin phototype. In the case of congenital naevi the melanoma risk is directly proportional to their size. For the development of the acquired naevi genetic factors appear to play more important role than the sun exposure. The exposure to sunlight can, however, result in the increasing number of naevi. According to various studies the protection with sunscreens is insufficient and, conversely, can lead to development of higher number of naevi. Relatively large number of naevocellular naevi can be often seen in patients with melanoma. Also the members of some families with familiar melanoma may develop increased number of (dysplastic) naevi. The evidence of familiar occurrence of melanoma is important for the identification of genetic factors which may play role in the melanoma initiation. Histopathologic evaluation of pigmented naevi belongs to the most complicated assessments in dermatopathology. The criteria used for lesions evaluation are not entirely specific and that is why some diagnostically relevant changes can be found in both benign and malignant lesions. It is, therefore, necessary to asses the all available data and to consider their mutual importance. The prevention of melanoma is of enormous importance and should particularly involve the patients with high numbers of pigmented, especially dysplastic naevi, patients with large congenital naevi, patients from the families with familiar melanoma and those who already had melanoma. This preventive care should be performed systematically by dermatologists.

Key words:
Pigmented naevi – melanoma – pigmentation – UV radiation


Zdroje

1. AUTIER, P., DORÉ, J. F., CATTARUZZA, M. S. et al. Sunscreen use, wearing clothes, and number of nevi in 6- to 7-year old European children. J. Nat. Cancer Inst., 1998, 90, p. 1873–1880.

2. BAUER J., BÜTTNER, P., WIECKER, TS. et al. Risk factors of incident melanocytic naevi: a longitudinal study in a cohort of 1232 young German children. Int. J. Cancer, 2005, 115, p. 121–126.

3. BAUER, J., GARBE, C. Acquired melanocytic nevi as risk factor for melanoma development. A comprehensive review of epidemiological data. Pigment Cell Res., 2003, 16, p. 297–306.

4. BROBERG, A., AUGUSTSSON, A. Atopic dermatitis and melanocytic naevi. Br. J. Dermatol., 2009, 142, p. 306–309.

5. CLARK, W. H, JR., REIEMER, R. R., GREENE, M. H. et al. Origin of familial melanomas from heritable melanocytic lesions. “The B-K mole syndrome”. Arch. Dermatol., 1978, 114, p. 732–738.

6. EASTON, D. F., COX, G. M., MACDONALD, A. M. et al. Genetic susceptibility to naevi – a twin study. Br. J. Cancer, 1991, 64, p. 1164–1167.

7. ELDER, D. E. Dysplastic naevi: an update. Histopathology, 2010, 56, p. 112–120.

8. FRIEDMAN, R. J., FARBER, M. J., WARYCHA, M. A. et al. The “dysplastic” nevus. Clin. Dermatol., 2009, 27, p.103–115.

9. GALLAGHER, R. P., MCLEAN, D. I., YANG, P. et al. Suntan, sunburn and pigmentation factors and the frequency of acquired melanocytic nevi in children. Arch. Dermatol., 1990, 126, p. 770–778.

10. GANDINI, S., SERA, F., CATARUZZA, M. S. et al. Meta-analysis of risk factors for cutaneous melanoma: I. Common and atypical naevi. Eur. J. Cancer, 2005, 41, p. 28–44.

11. HARRISON, S. L., MACLENNAN, R., SPEARE, R. et al. Sun exposure and melanocytic naevi in young Australian children. Lancet, 1994, 344, p. 1529–1532.

12. KINSLEY, V. A., CHONG, W. K., AYLETT, S. E. et al. Complications of congenital melanocytic naevi in children: analysis of 16 years‘ experience and clinical practice. Br. J. Dermatol., 2008, 159, p. 907–914.

13. LEECH, S. N., BELL, H., LEONARD, N. et al. Neonatal giant congenital naevi with proliferative nodules. Arch. Dermatol., 2004, 144, p. 83–88.

14. LIANG, X. S., PFEIFFER, R. M., WHEELER, W. et al. Genetic variants in DNA repair genes and the risk of cutaneous malignant melanoma in melanoma-prone families with/without CDKN2A mutations. Int. J. Cancer, 2011, v tisku.

15. MACKIE, R. M., ENGLISH, J., AITCHINSON, T. C. et al. The number and distribution of benign pigmented moles (melanocytic naevi) in a healthy British population. Br. J. Dermatol., 1985, 113, p. 167–174.

16. MAKKAR, H. S., FRIEDEN, I. J. Congenital melanocytic naevi: an update for the pediatrician. Curr. Opin. Pediatr., 2002, 14, p. 397–403.

17. MARGHOOB, A. A., BORREGO, J. P., HALPERN, A. C. Congenital melanocytic nevi: Treatment modalities and management options. Semin. Cutan. Med. Surg., 2007, 26, p. 231–240.

18. NIEUWPOORT van, F., SMIT, N. P. M., KOLB, A. M. et al. Tyrosine-induced melanogenesis shows differences in morphologic and melanogenic preferences of melanosomes from light and dark skin types. J. Invest. Dermatol., 2004, 122, p. 1251–1255.

19. PAVEL, S., NIEUWPOORT van, F., MEULEN VAN DER, J. et al. Disturbed melanin synthesis and chronic oxidative stress in melanoma precursor lesions. Eur. J. Cancer, 2004, 40, p. 1423–1430.

20. PAVEL, S., SMIT, N. P. M., MEULEN van der, J. et al. Homozygous germline mutation of the CDKN2A/p16 gene and G-6-PD deficiency in a multiple melanoma case. Melanoma Res., 2003, 13, p. 171–178.

21. PAVEL, S., SMIT, N. P. M., PIZINGER, K. Dysplastic nevi as precursor melanoma lesions. In J. Borovanský, P. A. Riley, editors. Melanins and Melanosomes: Biosynthesis, Biogenesis, Physiological, and Pathological Functions. First edition. Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim 2011, pp. 383–393.

22. RAEVE de, L. E., ROSEEUW, D. I. Curretage of giant congenital melanocytic nevi in neonates. Arch. Dermatol., 2002, 138, p. 943–948.

23. RHEE van der, J. I., KRIJNEN, P., GRUIS, N. A. et al. Clinical and histologic characteristics of malignant melanoma in families with a germline mutation in CDKN2A. J. Am. Acad. Dermatol., 2011, 65, p. 281–288.

24. RICHTING, E., LANGMANN, G., MULLNER, K. et al. Ocular melanoma: epidemiology, clinical presentation and relationship with dysplastic naevi. Ophthalmologica, 2004, 218, p. 111–114.

25. ROSS, A. L., SANCHEZ, M. L., GRINCHNIK, J. M. Molecular nevogenesis. Dermatology Research and Practice, 2011, v tisku.

26. SAGEBIEL, R. W. Melanocytic nevi in histologic association with primary cutaneous melanoma of superficial spreading and nodular types: effect of tumor thickness. J. Invest. Dermatol., 1993, 100, p. 322S–325S.

27. SCOPE, A., DUSZA, S. W., MARGHOOB, A. A. et al. Clinical and dermoscopic stability and volatility of melanocytic nevi in a population-based cohort of children in Framingham School System. J. Invest. Dermatol., 2011, 131, p. 1615–1621.

28. SMIT, N. P. M., KOLB, A. M., LENTJES, E. G. W. M. et al. Variations in melanin formation by cultured melanocytes from different skin types. Arch. Dermatol. Res., 1998, 290, p. 342–349.

29. SMIT, N. P. M., NIEUWPOORT van, F. A., MARROT, L. et al. Increased melanogenesis is a risk factor for oxidative DNA damage. Study on cultured melanocytes and atypical nevus cells. Photochem. Photobiol., 2008, 84, p. 550–555.

30. STINGO, G., ARGENZIANO, G., FAVOT, F. et al. Absence of clinical and dermoscopic differences between congenital and non-congenital melanocytic nevi in a cohort of two-year-old children. Br. J. Dermatol., 2011, v tisku.

31. SYNNERSTAD, I., NILSSON, L., FREDRIKSON, M. et al. Fewer melanocytic nevi found in children with active atopic dermatitis than in children without dermatitis. Arch. Dermatol., 2004, 140, p. 1471–1475.

32. WACHSMUTH, R. C., TURNER, F., BARRETT, J. H. et al. The effect of sun exposure in determining nevus density in UK adolescent twins. J. Invest. Dermatol., 2005, 124, p. 56–62.

33. WILLIAMS, M. L., PENNELLA, R. Melanoma, melanocytic nevi, and other melanoma risk factors in children. J. Pediatr., 1994, 104, p. 833–845.

34. WIESNER, T., OBENAUF, A. C., MURALI, R. et al. Germline mutations in BAP1 predispose to melanocytic tumors. Nature Gen., 2011, v tisku.

35. YOUL, P., AITKEN, J., HAYWARD, N. et al. Melanoma in adolescents: a case-control study of risk factors in Queensland, Australia. Int. J. Cancer, 2002, 98, p. 92–98.

Štítky
Dermatology & STDs Paediatric dermatology & STDs
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